Biallelic NAA60 variants with impaired n-terminal acetylation capacity cause autosomal recessive primary familial brain calcifications.

Autor: Chelban V; Department of Neuromuscular Diseases, UCL Queen Square Institute of Neurology, London, WC1N 3BG, UK. v.chelban@ucl.ac.uk.; Neurobiology and Medical Genetics Laboratory, 'Nicolae Testemitanu' State University of Medicine and Pharmacy, 165, Stefan cel Mare si Sfant Boulevard, MD, 2004, Chisinau, Republic of Moldova. v.chelban@ucl.ac.uk., Aksnes H; Department of Biomedicine, University of Bergen, Bergen, Norway. henriette.aksnes@uib.no., Maroofian R; Department of Neuromuscular Diseases, UCL Queen Square Institute of Neurology, London, WC1N 3BG, UK., LaMonica LC; Department of Cell Biology, Yale School of Medicine, New Haven, CT, USA., Seabra L; Université Paris Cité, Imagine Institute, Laboratory of Neurogenetics and Neuroinflammation, INSERM UMR 1163, Paris, France., Siggervåg A; Department of Biomedicine, University of Bergen, Bergen, Norway., Devic P; Hospices Civils de Lyon, Groupement Hospitalier Sud, Service d'Explorations Fonctionnelles Neurologiques, Lyon, France., Shamseldin HE; Department of Translational Genomics, Center for Genomic Medicine, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia., Vandrovcova J; Department of Neuromuscular Diseases, UCL Queen Square Institute of Neurology, London, WC1N 3BG, UK., Murphy D; Department of Clinical and Movement Neurosciences, UCL Queen Square Institute of Neurology, London, WC1N 3BG, UK., Richard AC; Univ Rouen Normandie, Inserm U1245, CHU Rouen, Department of Genetics and CNRMAJ, F-76000, Rouen, France., Quenez O; Univ Rouen Normandie, Inserm U1245, CHU Rouen, Department of Genetics and CNRMAJ, F-76000, Rouen, France., Bonnevalle A; Univ Rouen Normandie, Inserm U1245, CHU Rouen, Department of Genetics and CNRMAJ, F-76000, Rouen, France., Zanetti MN; Department of Clinical and Experimental Epilepsy, UCL Queen Square Institute of Neurology, London, WC1N 3BG, UK., Kaiyrzhanov R; Department of Neuromuscular Diseases, UCL Queen Square Institute of Neurology, London, WC1N 3BG, UK.; South Kazakhstan Medical Academy Shymkent, Shymkent, 160019, Kazakhstan., Salpietro V; Department of Neuromuscular Diseases, UCL Queen Square Institute of Neurology, London, WC1N 3BG, UK., Efthymiou S; Department of Neuromuscular Diseases, UCL Queen Square Institute of Neurology, London, WC1N 3BG, UK., Schottlaender LV; Department of Neuromuscular Diseases, UCL Queen Square Institute of Neurology, London, WC1N 3BG, UK.; Instituto de Investigaciones en Medicina Traslacional (IIMT), CONICET-Universidad Austral, Av. Juan Domingo Perón 1500, B1629AHJ, Pilar, Argentina.; Instituto de medicina genómica (IMeG), Hospital Universitario Austral, Universidad Austral, Av. Juan Domingo Perón 1500, B1629AHJ, Pilar, Argentina., Morsy H; Department of Neuromuscular Diseases, UCL Queen Square Institute of Neurology, London, WC1N 3BG, UK.; Department of Human Genetics, Medical Research Institute, Alexandria University, Alexandria, Egypt., Scardamaglia A; Department of Neuromuscular Diseases, UCL Queen Square Institute of Neurology, London, WC1N 3BG, UK., Tariq A; Department of Neuromuscular Diseases, UCL Queen Square Institute of Neurology, London, WC1N 3BG, UK., Pagnamenta AT; Oxford NIHR Biomedical Research Centre, Wellcome Centre for Human Genetics, Oxford, United Kingdom., Pennavaria A; Department of Biomedicine, University of Bergen, Bergen, Norway., Krogstad LS; Department of Biomedicine, University of Bergen, Bergen, Norway., Bekkelund ÅK; Department of Biomedicine, University of Bergen, Bergen, Norway., Caiella A; Department of Biomedicine, University of Bergen, Bergen, Norway., Glomnes N; Department of Biomedicine, University of Bergen, Bergen, Norway.; Department of Clinical Science, University of Bergen, 5020, Bergen, Norway., Brønstad KM; Department of Biomedicine, University of Bergen, Bergen, Norway., Tury S; Institut de Recherche en Infectiologie de Montpellier, Université de Montpellier, CNRS, Montpellier, France., Moreno De Luca A; Department of Radiology, Autism & Developmental Medicine Institute, Geisinger, Lewisburg, PA, USA.; Department of Radiology, Neuroradiology Section, Kingston Health Sciences Centre, Queen's University Faculty of Health Sciences, Kingston, Ontario, Canada., Boland-Auge A; Université Paris-Saclay, CEA, Centre National de Recherche en Génomique Humaine (CNRGH), 91057, Evry, France., Olaso R; Université Paris-Saclay, CEA, Centre National de Recherche en Génomique Humaine (CNRGH), 91057, Evry, France., Deleuze JF; Université Paris-Saclay, CEA, Centre National de Recherche en Génomique Humaine (CNRGH), 91057, Evry, France., Anheim M; Neurology Department, Strasbourg University Hospital, Strasbourg, France.; Strasbourg Federation of Translational Medicine (FMTS), Strasbourg University, Strasbourg, France.; INSERM-U964; CNRS-UMR7104, University of Strasbourg, Illkirch-Graffenstaden, France., Cretin B; Neurology Department, Strasbourg University Hospital, Strasbourg, France.; Strasbourg Federation of Translational Medicine (FMTS), Strasbourg University, Strasbourg, France.; INSERM-U964; CNRS-UMR7104, University of Strasbourg, Illkirch-Graffenstaden, France., Vona B; Institute of Human Genetics, University Medical Center Göttingen, 37073, Göttingen, Germany.; Institute for Auditory Neuroscience and InnerEarLab, University Medical Center Göttingen, 37075, Göttingen, Germany., Alajlan F; Department of Neuroscience Center, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia., Abdulwahab F; Department of Translational Genomics, Center for Genomic Medicine, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia., Battini JL; Institut de Recherche en Infectiologie de Montpellier, Université de Montpellier, CNRS, Montpellier, France., İpek R; Paediatric Neurology, Faculty of Medicine, Dicle University, Diyarbakır, Turkey., Bauer P; Centogene GmbH, Am Strande 7, 18055, Rostock, Germany., Zifarelli G; Centogene GmbH, Am Strande 7, 18055, Rostock, Germany., Gungor S; Inonu University, Faculty of Medicine, Turgut Ozal Research Center, Department of Pediatrics, Division of Pediatric Neurology, Malatya, Turkey., Kurul SH; Dokuz Eylul University, School of Medicine, Department of Paediatric Neurology, Izmir, Turkey., Lochmuller H; Children's Hospital of Eastern Ontario Research Institute and Division of Neurology, Department of Medicine, The Ottawa Hospital, Ottawa, Canada.; Brain and Mind Research Institute, University of Ottawa, Ottawa, Canada.; Department of Neuropediatrics and Muscle Disorders, Medical Center-University of Freiburg, Faculty of Medicine, Freiburg, Germany., Da'as SI; Department of Human Genetics, Sidra Medicine, Doha, Qatar.; College of Health and Life Sciences, Hamad Bin Khalifa University, Doha, Qatar., Fakhro KA; Department of Human Genetics, Sidra Medicine, Doha, Qatar.; College of Health and Life Sciences, Hamad Bin Khalifa University, Doha, Qatar.; Weill Cornell Medical College, Doha, Qatar., Gómez-Pascual A; Department of Information and Communications Engineering, University of Murcia, Campus Espinardo, 30100, Murcia, Spain., Botía JA; Department of Information and Communications Engineering, University of Murcia, Campus Espinardo, 30100, Murcia, Spain., Wood NW; Department of Clinical and Movement Neurosciences, UCL Queen Square Institute of Neurology, London, WC1N 3BG, UK.; Neurogenetics Laboratory, The National Hospital for Neurology and Neurosurgery, London, WC1N 3BG, UK., Horvath R; Department of Clinical Neurosciences, University of Cambridge, Cambridge, UK., Ernst AM; Department of Cell Biology, Yale School of Medicine, New Haven, CT, USA.; School of Biological Sciences, Department of Cell and Developmental Biology, University of California San Diego, La Jolla, CA, USA., Rothman JE; Department of Cell Biology, Yale School of Medicine, New Haven, CT, USA.; Department of Clinical and Experimental Epilepsy, UCL Queen Square Institute of Neurology, London, WC1N 3BG, UK., McEntagart M; Medical Genetics Department, St George's University Hospitals, London, SWI7 0RE, UK., Crow YJ; Université Paris Cité, Imagine Institute, Laboratory of Neurogenetics and Neuroinflammation, INSERM UMR 1163, Paris, France.; MRC Human Genetics Unit, Institute of Genetics and Cancer, University of Edinburgh, Edinburgh, UK., Alkuraya FS; Department of Translational Genomics, Center for Genomic Medicine, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.; Department of Anatomy and Cell Biology, College of Medicine, Alfaisal University, Riyadh, Saudi Arabia., Nicolas G; Univ Rouen Normandie, Inserm U1245, CHU Rouen, Department of Genetics and CNRMAJ, F-76000, Rouen, France., Arnesen T; Department of Biomedicine, University of Bergen, Bergen, Norway. thomas.arnesen@uib.no.; Department of Surgery, Haukeland University Hospital, Bergen, Norway. thomas.arnesen@uib.no., Houlden H; Department of Neuromuscular Diseases, UCL Queen Square Institute of Neurology, London, WC1N 3BG, UK. h.houlden@ucl.ac.uk.; Neurogenetics Laboratory, The National Hospital for Neurology and Neurosurgery, London, WC1N 3BG, UK. h.houlden@ucl.ac.uk.

Publikováno v: Nature communications [Nat Commun] 2024 Mar 13; Vol. 15 (1), pp. 2269. Date of Electronic Publication: 2024 Mar 13.

Early-infantile onset epilepsy and developmental delay caused by bi-allelic GAD1 variants.

Autor: Neuray C; UCL Queen Square Institute of Neurology, University College London, London, UK.; Department of Neurology, Christian Doppler Klinik, Paracelsus Medical University, Salzburg, Austria., Maroofian R; UCL Queen Square Institute of Neurology, University College London, London, UK., Scala M; UCL Queen Square Institute of Neurology, University College London, London, UK.; Department of Neurosciences, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health, University of Genoa, Genoa, Italy.; IRCCS Istituto Giannina Gaslini, Genoa, Italy., Sultan T; Department of Pediatric Neurology, Children's Hospital and Institute of Child Health, Lahore, Pakistan., Pai GS; Medical University of South Carolina, USA., Mojarrad M; Department of Medical Genetics, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran.; Medical Genetics Research Center, Mashhad University of Medical Sciences, Mashhad, Iran.; Genetic Center of Khorasan Razavi, Mashhad, Iran., Khashab HE; Department of Pediatrics, Children's Hospital, Ain Shams University, Cairo, Egypt.; Department of Pediatrics, Dr. Suliman Al Habib Medical Group, Riyadh, Saudi Arabia., deHoll L; Medical University of South Carolina, USA., Yue W; Structural Genomics Consortium, Nuffield Department of Clinical Medicine, University of Oxford, UK., Alsaif HS; Student Research Committee, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran., Zanetti MN; Department of Clinical and Experimental Epilepsy, University College London, London, UK., Bello O; Department of Clinical and Experimental Epilepsy, University College London, London, UK., Person R; GeneDx, Gaithersburg, MD, USA., Eslahi A; Department of Medical Genetics, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran.; Student Research Committee, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran., Khazaei Z; Genetic Center of Khorasan Razavi, Mashhad, Iran., Feizabadi MH; Department of Medical Genetics, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran., Efthymiou S; UCL Queen Square Institute of Neurology, University College London, London, UK., El-Bassyouni HT; Clinical Genetics Department, National Research Centre, Cairo, Egypt., Soliman DR; Department of Pediatrics, Faculty of Medicine, Benha University, Benha, Egypt., Tekes S; Dicle University, School of Medicine, Department of Medical Genetics, Diyarbakir, Turkey., Ozer L; Yuksek Ihtisas University, School of Medicine, Department of Medical Genetics, Ankara, Turkey., Baltaci V; Mikrogen Genetic Diagnosis Center, Ankara, Turkey., Khan S; CENTOGENE AG, Rostock., Beetz C; CENTOGENE AG, Rostock., Amr KS; Molecular Genetics Department, National Research Centre, Cairo, Egypt., Salpietro V; UCL Queen Square Institute of Neurology, University College London, London, UK., Jamshidi Y; Molecular and Clinical Sciences Institute St George's, University of London, UK., Alkuraya FS; Department of Genetics, King Faisal Specialist Hospital and Research Center Riyadh, Saudi Arabia., Houlden H; UCL Queen Square Institute of Neurology, University College London, London, UK.

Publikováno v: Brain : a journal of neurology [Brain] 2020 Aug 01; Vol. 143 (8), pp. 2388-2397.

PDXK mutations cause polyneuropathy responsive to pyridoxal 5'-phosphate supplementation.

Autor: Chelban V; Department of Neuromuscular Diseases, University College London Queen Square Institute of Neurology, London, United Kingdom.; Department of Neurology and Neurosurgery, Institute of Emergency Medicine, Chisinau, Moldova., Wilson MP; Genetics and Genomic Medicine, University College London Great Ormond Street Institute of Child Health, London, United Kingdom., Warman Chardon J; Department of Medicine (Neurology), University of Ottawa, Ottawa, Ontario, Canada.; Ottawa Hospital Research Institute, Ottawa, Ontario, Canada.; Children's Hospital of Eastern Ontario Research Institute, University of Ottawa, Ottawa, Ontario, Canada., Vandrovcova J; Department of Neuromuscular Diseases, University College London Queen Square Institute of Neurology, London, United Kingdom., Zanetti MN; Department of Clinical and Experimental Epilepsy, University College London Queen Square Institute of Neurology, London, United Kingdom., Zamba-Papanicolaou E; Cyprus Institute of Neurology and Genetics, Nicosia, Cyprus.; Cyprus School of Molecular Medicine, Nicosia, Cyprus., Efthymiou S; Department of Neuromuscular Diseases, University College London Queen Square Institute of Neurology, London, United Kingdom., Pope S; Neurometabolic Unit, National Hospital for Neurology and Neurosurgery, London, United Kingdom., Conte MR; Randall Centre of Cell and Molecular Biophysics, School of Basic and Medical Biosciences, King's College London, London, United Kingdom., Abis G; Randall Centre of Cell and Molecular Biophysics, School of Basic and Medical Biosciences, King's College London, London, United Kingdom., Liu YT; Department of Neurology, Neurological Institute, Taipei Veterans General Hospital, Taipei, Taiwan.; National Yang-Ming University School of Medicine, Taipei, Taiwan.; Institute of Brain Science, National Yang-Ming University, Taipei, Taiwan., Tribollet E; Department of Neuromuscular Diseases, University College London Queen Square Institute of Neurology, London, United Kingdom., Haridy NA; Department of Neuromuscular Diseases, University College London Queen Square Institute of Neurology, London, United Kingdom.; Department of Neurology and Psychiatry, Assiut University Hospital, Faculty of Medicine, Asyut, Egypt., Botía JA; Reta Lila Weston Research Laboratories, University College London Queen Square Institute of Neurology, London, United Kingdom.; Department of Information and Communications Engineering, University of Murcia, Murcia, Spain., Ryten M; Reta Lila Weston Research Laboratories, University College London Queen Square Institute of Neurology, London, United Kingdom.; Department of Medical & Molecular Genetics, King's College London, Guy's Hospital, London, United Kingdom., Nicolaou P; Cyprus Institute of Neurology and Genetics, Nicosia, Cyprus.; Cyprus School of Molecular Medicine, Nicosia, Cyprus., Minaidou A; Cyprus Institute of Neurology and Genetics, Nicosia, Cyprus.; Cyprus School of Molecular Medicine, Nicosia, Cyprus., Christodoulou K; Cyprus Institute of Neurology and Genetics, Nicosia, Cyprus.; Cyprus School of Molecular Medicine, Nicosia, Cyprus., Kernohan KD; Children's Hospital of Eastern Ontario Research Institute, University of Ottawa, Ottawa, Ontario, Canada.; Newborn Screening Ontario, Children's Hospital of Eastern Ontario, Ottawa, Ontario, Canada., Eaton A; Children's Hospital of Eastern Ontario Research Institute, University of Ottawa, Ottawa, Ontario, Canada., Osmond M; Children's Hospital of Eastern Ontario Research Institute, University of Ottawa, Ottawa, Ontario, Canada., Ito Y; Children's Hospital of Eastern Ontario Research Institute, University of Ottawa, Ottawa, Ontario, Canada., Bourque P; Department of Medicine (Neurology), University of Ottawa, Ottawa, Ontario, Canada.; Ottawa Hospital Research Institute, Ottawa, Ontario, Canada., Jepson JEC; Department of Clinical and Experimental Epilepsy, University College London Queen Square Institute of Neurology, London, United Kingdom., Bello O; Department of Clinical and Experimental Epilepsy, University College London Queen Square Institute of Neurology, London, United Kingdom., Bremner F; Neuro-ophthalmology Department, National Hospital for Neurology and Neurosurgery, London, United Kingdom., Cordivari C; Clinical Neurophysiology Department, National Hospital for Neurology and Neurosurgery, London, United Kingdom., Reilly MM; Department of Neuromuscular Diseases, University College London Queen Square Institute of Neurology, London, United Kingdom., Foiani M; Clinical Neurophysiology Department, National Hospital for Neurology and Neurosurgery, London, United Kingdom.; Department of Neurodegenerative Disease, University College London Queen Square Institute of Neurology, London, United Kingdom., Heslegrave A; Department of Neurodegenerative Disease, University College London Queen Square Institute of Neurology, London, United Kingdom.; UK Dementia Research Institute at University College London, London, United Kingdom., Zetterberg H; Department of Neurodegenerative Disease, University College London Queen Square Institute of Neurology, London, United Kingdom.; UK Dementia Research Institute at University College London, London, United Kingdom.; Clinical Neurochemistry Laboratory, Sahlgrenska University Hospital, Mölndal, Sweden.; Department of Psychiatry and Neurochemistry, Institute of Neuroscience and Physiology, Sahlgrenska Academy at University of Gothenburg, Mölndal, Sweden., Heales SJR; Neurometabolic Unit, National Hospital for Neurology and Neurosurgery, London, United Kingdom., Wood NW; Department of Neuromuscular Diseases, University College London Queen Square Institute of Neurology, London, United Kingdom.; Neurogenetics Laboratory, National Hospital for Neurology and Neurosurgery, London, United Kingdom., Rothman JE; Department of Clinical and Experimental Epilepsy, University College London Queen Square Institute of Neurology, London, United Kingdom.; Department of Cell Biology, Yale School of Medicine, New Haven, CT., Boycott KM; Children's Hospital of Eastern Ontario Research Institute, University of Ottawa, Ottawa, Ontario, Canada., Mills PB; Genetics and Genomic Medicine, University College London Great Ormond Street Institute of Child Health, London, United Kingdom., Clayton PT; Genetics and Genomic Medicine, University College London Great Ormond Street Institute of Child Health, London, United Kingdom., Houlden H; Department of Neuromuscular Diseases, University College London Queen Square Institute of Neurology, London, United Kingdom.; Neurogenetics Laboratory, National Hospital for Neurology and Neurosurgery, London, United Kingdom.

Publikováno v: Annals of neurology [Ann Neurol] 2019 Aug; Vol. 86 (2), pp. 225-240. Date of Electronic Publication: 2019 Jul 01.

Mutations in NKX6-2 Cause Progressive Spastic Ataxia and Hypomyelination.

Autor: Chelban V; Department of Molecular Neuroscience, University College London, London WC1N 3BG, UK; Department of Neurology and Neurosurgery, Institute of Emergency Medicine, Toma Ciorbă 1, 2052 Chisinau, Republic of Moldova. Electronic address: v.chelban@ucl.ac.uk., Patel N; Developmental Genetics Unit, Department of Genetics, King Faisal Specialist Hospital and Research Center, MBC 03, PO Box 3354, Riyadh 11211 Saudi Arabia., Vandrovcova J; Department of Molecular Neuroscience, University College London, London WC1N 3BG, UK., Zanetti MN; Department of Clinical and Experimental Epilepsy, University College London, London WC1N 3BG, UK., Lynch DS; Department of Molecular Neuroscience, University College London, London WC1N 3BG, UK., Ryten M; Reta Lila Weston Research Laboratories, Institute of Neurology, University College London, London WC1N 3BG, UK; Department of Medical and Molecular Genetics, King's College London, Guy's Hospital, SE1 9RT London, UK., Botía JA; Reta Lila Weston Research Laboratories, Institute of Neurology, University College London, London WC1N 3BG, UK; Department of Information and Communications Engineering, University of Murcia, Campus Espinardo, 30100 Murcia, Spain., Bello O; Department of Clinical and Experimental Epilepsy, University College London, London WC1N 3BG, UK., Tribollet E; Department of Molecular Neuroscience, University College London, London WC1N 3BG, UK., Efthymiou S; Department of Molecular Neuroscience, University College London, London WC1N 3BG, UK., Davagnanam I; Department of Brain Repair and Rehabilitation, University College London, London WC1N 3BG, UK., Bashiri FA; Department of Pediatrics, College of Medicine, King Saud University, Riyadh 11451, Saudi Arabia., Wood NW; Department of Molecular Neuroscience, University College London, London WC1N 3BG, UK; Neurogenetics Laboratory, The National Hospital for Neurology and Neurosurgery, London WC1N 3BG, UK., Rothman JE; Department of Clinical and Experimental Epilepsy, University College London, London WC1N 3BG, UK; Department of Cell Biology, Yale School of Medicine, New Haven, CT 06520-8002., Alkuraya FS; Developmental Genetics Unit, Department of Genetics, King Faisal Specialist Hospital and Research Center, MBC 03, PO Box 3354, Riyadh 11211 Saudi Arabia; Department of Anatomy and Cell Biology, College of Medicine, Alfaisal University, Riyadh 11533, Saudi Arabia; Saudi Human Genome Program, King Abdulaziz City for Science and Technology, Riyadh 12371, Saudi Arabia. Electronic address: falkuraya@kfshrc.edu.sa., Houlden H; Department of Molecular Neuroscience, University College London, London WC1N 3BG, UK; Neurogenetics Laboratory, The National Hospital for Neurology and Neurosurgery, London WC1N 3BG, UK.

Publikováno v: American journal of human genetics [Am J Hum Genet] 2017 Jun 01; Vol. 100 (6), pp. 969-977.

Rab3A, a possible marker of cortical granules, participates in cortical granule exocytosis in mouse eggs.

Autor: Bello OD; Instituto de Histología y Embriología, CONICET - Universidad Nacional de Cuyo, Av. Libertador 80, 5500 Mendoza, Argentina., Cappa AI; Instituto de Histología y Embriología, CONICET - Universidad Nacional de Cuyo, Av. Libertador 80, 5500 Mendoza, Argentina., de Paola M; Instituto de Histología y Embriología, CONICET - Universidad Nacional de Cuyo, Av. Libertador 80, 5500 Mendoza, Argentina., Zanetti MN; Instituto de Histología y Embriología, CONICET - Universidad Nacional de Cuyo, Av. Libertador 80, 5500 Mendoza, Argentina., Fukuda M; Department of Developmental Biology and Neurosciences, Graduate School of Life Sciences, Tohoku University, Sendai, Miyagi 980-8578, Japan., Fissore RA; Department of Veterinary and Animal Sciences, University of Massachusetts Amherst, 661 North Pleasant Street, Amherst, MA 01003, USA., Mayorga LS; Instituto de Histología y Embriología, CONICET - Universidad Nacional de Cuyo, Av. Libertador 80, 5500 Mendoza, Argentina., Michaut MA; Instituto de Histología y Embriología, CONICET - Universidad Nacional de Cuyo, Av. Libertador 80, 5500 Mendoza, Argentina; Facultad de Ciencias Exactas y Naturales, Universidad Nacional de Cuyo, Argentina. Electronic address: mmichaut@gmail.com.

Publikováno v: Experimental cell research [Exp Cell Res] 2016 Sep 10; Vol. 347 (1), pp. 42-51. Date of Electronic Publication: 2016 Jul 14.