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
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
532Commentaires et corrections
Type : ErratumFor