A Novel
Colombia
WHSUS
case report
neurodevelopmental disorder
Journal
The application of clinical genetics
ISSN: 1178-704X
Titre abrégé: Appl Clin Genet
Pays: New Zealand
ID NLM: 101579789
Informations de publication
Date de publication:
2022
2022
Historique:
received:
05
04
2022
accepted:
08
06
2022
entrez:
13
7
2022
pubmed:
14
7
2022
medline:
14
7
2022
Statut:
epublish
Résumé
White-Sutton syndrome is a rare type of autosomal dominant neurodevelopmental disorder caused by mutations, mostly
Identifiants
pubmed: 35821784
doi: 10.2147/TACG.S369483
pii: 369483
pmc: PMC9271277
doi:
Types de publication
Case Reports
Langues
eng
Pagination
63-68Informations de copyright
© 2022 Giraldo-Ocampo et al.
Déclaration de conflit d'intérêts
The authors report no conflicts of interest in relation to this work.
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