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Correction: Phenotypic spectrum associated with a CRADD founder variant underlying frontotemporal predominant pachygyria in the Finnish population.
Polla, Daniel L; Rahikkala, Elisa; Bode, Michaela K; Määttä, Tuomo; Varilo, Teppo; Loman, Thyrza; Philips, Anju K; Kurki, Mitja; Palotie, Aarno; Körkkö, Jarmo; Vieira, Päivi; Avela, Kristiina; Jacquemin, Valérie; Pirson, Isabelle; Abramowicz, Marc; de Brouwer, Arjan P M; Kuismin, Outi; van Bokhoven, Hans; Järvelä, Irma.
Afiliación
  • Polla DL; Department of Human Genetics, Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Center, Nijmegen, The Netherlands.
  • Rahikkala E; CAPES Foundation, Ministry of Education of Brazil, Brasília, Brazil.
  • Bode MK; Department of Clinical Genetics, PEDEGO Research Unit and Medical Research Center Oulu, Oulu University Hospital and University of Oulu, Oulu, Finland.
  • Määttä T; Department of Diagnostic Radiology, Oulu University Hospital and Medical Research Center Oulu, Oulu, Finland.
  • Varilo T; Disability Services, Joint Authority for Kainuu, Kainuu, Finland.
  • Loman T; Department of Medical Genetics, University of Helsinki, Helsinki, Finland.
  • Philips AK; Department of Human Genetics, Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Center, Nijmegen, The Netherlands.
  • Kurki M; Department of Medical Genetics, University of Helsinki, Helsinki, Finland.
  • Palotie A; Psychiatric & Neurodevelopmental Genetics Unit, Massachusetts General Hospital, Boston, MA, USA.
  • Körkkö J; The Stanley Center for Psychiatric Research, The Broad Institute of MIT and Harvard, Cambridge, MA, USA.
  • Vieira P; Institute for Molecular Medicine Finland (FIMM), University of Helsinki, Helsinki, Finland.
  • Avela K; Psychiatric & Neurodevelopmental Genetics Unit, Massachusetts General Hospital, Boston, MA, USA.
  • Jacquemin V; The Stanley Center for Psychiatric Research, The Broad Institute of MIT and Harvard, Cambridge, MA, USA.
  • Pirson I; Institute for Molecular Medicine Finland (FIMM), University of Helsinki, Helsinki, Finland.
  • Abramowicz M; Analytic and Translational Genetics Unit, Department of Medicine, Massachusetts General Hospital, Boston, MA, USA.
  • de Brouwer APM; Department of Neurology, Massachusetts General Hospital, Boston, MA, USA.
  • Kuismin O; Northern Ostrobothnia Hospital District, Center for Intellectual Disability Care, 90220, Oulu, Finland.
  • van Bokhoven H; Clinic for Children and Adolescents, PEDEGO Research Unit and Medical Research Center Oulu, Oulu University Hospital and University of Oulu, Oulu, Finland.
  • Järvelä I; Department of Clinical Genetics, Helsinki University Hospital, Helsinki, Finland.
Eur J Hum Genet ; 28(4): 532, 2020 Apr.
Article en En | MEDLINE | ID: mdl-31506600
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Tipo de estudio: Risk_factors_studies Idioma: En Revista: Eur J Hum Genet Asunto de la revista: GENETICA MEDICA Año: 2020 Tipo del documento: Article País de afiliación: Países Bajos
Texto completo
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Tipo de estudio: Risk_factors_studies Idioma: En Revista: Eur J Hum Genet Asunto de la revista: GENETICA MEDICA Año: 2020 Tipo del documento: Article País de afiliación: Países Bajos