Single and multiple point NRAS mutations in acute myeloid leukemia: a study of 327 well molecularly characterized patients.

Autor: Durinikova, Anna^1,2 (AUTHOR), Folta, Adam¹ (AUTHOR), Pardy, Filip³ (AUTHOR), Svaton, Jan^1,3 (AUTHOR), Drncova, Marie^1,2 (AUTHOR), Weinbergerova, Barbora^1,2 (AUTHOR), Cetkovsky, Petr⁴ (AUTHOR), Racil, Zdenek⁴ (AUTHOR), Jindra, Pavel⁵ (AUTHOR), Szotkowski, Tomas⁶ (AUTHOR), Zak, Pavel⁷ (AUTHOR), Mayer, Jiri^1,2,3 (AUTHOR), Jeziskova, Ivana^1,2 (AUTHOR)

Publikováno v: Leukemia & Lymphoma. Dec2022, Vol. 63 Issue 13, p3237-3240. 4p.

First report of MEFV gene duplication in a patient with familial Mediterranean fever

Autor: Mechin, Déborah, Durinikova, Anna, Boursier, Guilaine, Andre, Marc, Touitou, Isabelle, Sarrabay, Guillaume

Publikováno v: Clinical and experimental rheumatology
Clinical and experimental rheumatology, Clinical and Experimental Rheumatology Sas, 2020, 38 (5, suppl.127), pp.129-130
Clinical and experimental rheumatology, 2020, 38 (5, suppl.127), pp.129-130

International audience

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::a598bfb5447f5d884f5fd2fccc7301dc
https://hal.umontpellier.fr/hal-03176539

First report of MEFV gene duplication in a patient with familial Mediterranean fever.

Autor: Mechin D; CHU Montpellier, University of Montpellier, Department of Medical Genetics, Rare Diseases and Personalized Medicine, Rare and Autoinflammatory Diseases Unit, CEREMAIA Reference Centre, Montpellier, and IRMB, University of Montpellier, INSERM, CHU Montpellier, France., Durinikova A; CHU Montpellier, University of Montpellier, Department of Medical Genetics, Rare Diseases and Personalized Medicine, Rare and Autoinflammatory Diseases Unit, CEREMAIA Reference Centre, Montpellier, France., Boursier G; CHU Montpellier, University of Montpellier, Department of Medical Genetics, Rare Diseases and Personalized Medicine, Rare and Autoinflammatory Diseases Unit, CEREMAIA Reference Centre, Montpellier, France., André M; CHU Clermont-Ferrand, Service de Médecine Interne, Hôpital Gabriel Montpied, Clermont-Ferrand, and Université Clermont Auvergne, Inserm U1071, INRA USC2018, M2iSH, Clermont-Ferrand, France., Touitou I; CHU Montpellier, University of Montpellier, Department of Medical Genetics, Rare Diseases and Personalized Medicine, Rare and Autoinflammatory Diseases Unit, CEREMAIA Reference Centre, Montpellier, and IRMB, University of Montpellier, INSERM, CHU Montpellier, France., Sarrabay G; CHU Montpellier, University of Montpellier, Department of Medical Genetics, Rare Diseases and Personalized Medicine, Rare and Autoinflammatory Diseases Unit, CEREMAIA Reference Centre, Montpellier, and IRMB, University of Montpellier, INSERM, CHU Montpellier, France. guillaume.sarrabay@inserm.fr.

Publikováno v: Clinical and experimental rheumatology [Clin Exp Rheumatol] 2020 Sep-Oct; Vol. 38 Suppl 127 (5), pp. 129-130. Date of Electronic Publication: 2020 Dec 10.