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


Journal

European journal of human genetics : EJHG
ISSN: 1476-5438
Titre abrégé: Eur J Hum Genet
Pays: England
ID NLM: 9302235

Informations de publication

Date de publication:
Apr 2020
Historique:
pubmed: 12 9 2019
medline: 12 9 2019
entrez: 12 9 2019
Statut: ppublish

Résumé

An amendment to this paper has been published and can be accessed via a link at the top of the paper.

Identifiants

pubmed: 31506600
doi: 10.1038/s41431-019-0491-5
pii: 10.1038/s41431-019-0491-5
pmc: PMC7080772
doi:

Types de publication

Published Erratum

Langues

eng

Sous-ensembles de citation

IM

Pagination

532

Commentaires et corrections

Type : ErratumFor

Auteurs

Daniel L 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.

Elisa Rahikkala (E)

Department of Clinical Genetics, PEDEGO Research Unit and Medical Research Center Oulu, Oulu University Hospital and University of Oulu, Oulu, Finland.

Michaela K Bode (MK)

Department of Diagnostic Radiology, Oulu University Hospital and Medical Research Center Oulu, Oulu, Finland.

Tuomo Määttä (T)

Disability Services, Joint Authority for Kainuu, Kainuu, Finland.

Teppo Varilo (T)

Department of Medical Genetics, University of Helsinki, Helsinki, Finland.

Thyrza Loman (T)

Department of Human Genetics, Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Center, Nijmegen, The Netherlands.

Anju K Philips (AK)

Department of Medical Genetics, University of Helsinki, Helsinki, Finland.

Mitja 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.

Aarno 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.

Jarmo Körkkö (J)

Northern Ostrobothnia Hospital District, Center for Intellectual Disability Care, 90220, Oulu, Finland.

Päivi Vieira (P)

Clinic for Children and Adolescents, PEDEGO Research Unit and Medical Research Center Oulu, Oulu University Hospital and University of Oulu, Oulu, Finland.

Kristiina Avela (K)

Department of Clinical Genetics, Helsinki University Hospital, Helsinki, Finland.

Valérie Jacquemin (V)

Medical Genetics, IRIBHM, Université Libre de Bruxelles, Brussels, Belgium.

Isabelle Pirson (I)

Medical Genetics, IRIBHM, Université Libre de Bruxelles, Brussels, Belgium.

Marc Abramowicz (M)

Medical Genetics, IRIBHM, Université Libre de Bruxelles, Brussels, Belgium.

Arjan P M de Brouwer (APM)

Department of Human Genetics, Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Center, Nijmegen, The Netherlands.

Outi 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.

Hans van Bokhoven (H)

Department of Human Genetics, Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Center, Nijmegen, The Netherlands.

Irma Järvelä (I)

Department of Medical Genetics, University of Helsinki, Helsinki, Finland. irma.jarvela@helsinki.fi.

Classifications MeSH