Significant phenotypic variability in a multigenerational family with an
NFIA‐related disorder
corpus callosum hypoplasia
developmental delay
macrocephaly
nuclear factor I
Journal
Clinical case reports
ISSN: 2050-0904
Titre abrégé: Clin Case Rep
Pays: England
ID NLM: 101620385
Informations de publication
Date de publication:
Jan 2024
Jan 2024
Historique:
received:
21
09
2023
revised:
09
11
2023
accepted:
18
11
2023
medline:
8
1
2024
pubmed:
8
1
2024
entrez:
8
1
2024
Statut:
epublish
Résumé
We report the first multigenerational family with
Identifiants
pubmed: 38188845
doi: 10.1002/ccr3.8307
pii: CCR38307
pmc: PMC10769898
doi:
Types de publication
Case Reports
Langues
eng
Pagination
e8307Informations de copyright
© 2024 The Authors. Clinical Case Reports published by John Wiley & Sons Ltd.
Déclaration de conflit d'intérêts
The authors declare no competing interests in relation to this study.