Correction: Phenotypic spectrum associated with a CRADD founder variant underlying frontotemporal predominant pachygyria in the Finnish population.

Autor: Polla DL; Department of Human Genetics, Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Center, Nijmegen, The Netherlands.; CAPES Foundation, Ministry of Education of Brazil, Brasília, Brazil., Rahikkala E; Department of Clinical Genetics, PEDEGO Research Unit and Medical Research Center Oulu, Oulu University Hospital and University of Oulu, Oulu, Finland., Bode MK; Department of Diagnostic Radiology, Oulu University Hospital and Medical Research Center Oulu, Oulu, Finland., Määttä T; Disability Services, Joint Authority for Kainuu, Kainuu, Finland., Varilo T; Department of Medical Genetics, University of Helsinki, Helsinki, Finland., Loman T; Department of Human Genetics, Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Center, Nijmegen, The Netherlands., Philips AK; Department of Medical Genetics, University of Helsinki, Helsinki, Finland., Kurki M; Psychiatric & Neurodevelopmental Genetics Unit, Massachusetts General Hospital, Boston, MA, USA.; The Stanley Center for Psychiatric Research, The Broad Institute of MIT and Harvard, Cambridge, MA, USA.; Institute for Molecular Medicine Finland (FIMM), University of Helsinki, Helsinki, Finland., Palotie A; Psychiatric & Neurodevelopmental Genetics Unit, Massachusetts General Hospital, Boston, MA, USA.; The Stanley Center for Psychiatric Research, The Broad Institute of MIT and Harvard, Cambridge, MA, USA.; Institute for Molecular Medicine Finland (FIMM), University of Helsinki, Helsinki, Finland.; Analytic and Translational Genetics Unit, Department of Medicine, Massachusetts General Hospital, Boston, MA, USA.; Department of Neurology, Massachusetts General Hospital, Boston, MA, USA., Körkkö J; Northern Ostrobothnia Hospital District, Center for Intellectual Disability Care, 90220, Oulu, Finland., Vieira P; Clinic for Children and Adolescents, PEDEGO Research Unit and Medical Research Center Oulu, Oulu University Hospital and University of Oulu, Oulu, Finland., Avela K; Department of Clinical Genetics, Helsinki University Hospital, Helsinki, Finland., Jacquemin V; Medical Genetics, IRIBHM, Université Libre de Bruxelles, Brussels, Belgium., Pirson I; Medical Genetics, IRIBHM, Université Libre de Bruxelles, Brussels, Belgium., Abramowicz M; Medical Genetics, IRIBHM, Université Libre de Bruxelles, Brussels, Belgium., de Brouwer APM; Department of Human Genetics, Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Center, Nijmegen, The Netherlands., Kuismin O; Department of Clinical Genetics, PEDEGO Research Unit and Medical Research Center Oulu, Oulu University Hospital and University of Oulu, Oulu, Finland.; Institute for Molecular Medicine Finland (FIMM), University of Helsinki, Helsinki, Finland., van Bokhoven H; Department of Human Genetics, Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Center, Nijmegen, The Netherlands., Järvelä I; Department of Medical Genetics, University of Helsinki, Helsinki, Finland. irma.jarvela@helsinki.fi.
Jazyk: angličtina
Zdroj: European journal of human genetics : EJHG [Eur J Hum Genet] 2020 Apr; Vol. 28 (4), pp. 532.
DOI: 10.1038/s41431-019-0491-5
Abstrakt: An amendment to this paper has been published and can be accessed via a link at the top of the paper.
Databáze: MEDLINE