Correction: DPH1 syndrome: two novel variants and structural and functional analyses of seven missense variants identified in syndromic patients.
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:
Jan 2020
Jan 2020
Historique:
pubmed:
4
9
2019
medline:
4
9
2019
entrez:
4
9
2019
Statut:
ppublish
Résumé
Following the publication of the article, it was noted that the last column in Table 1, the total % should have read 5/8 (62.5) for the 'Epilepsy' row, and not 5.7 (71.4). This has now been amended in the HTML and PDF of the original article.
Identifiants
pubmed: 31477843
doi: 10.1038/s41431-019-0394-5
pii: 10.1038/s41431-019-0394-5
pmc: PMC6906502
doi:
Types de publication
Published Erratum
Langues
eng
Sous-ensembles de citation
IM
Pagination
138Commentaires et corrections
Type : ErratumFor