Deletion of
Gtf2i
PHP.eB serotype
Williams syndrome (WS)
adeno-associated virus (AAV)
excitatory neurons
post-natal deletion
social behavior
Journal
Biomedicines
ISSN: 2227-9059
Titre abrégé: Biomedicines
Pays: Switzerland
ID NLM: 101691304
Informations de publication
Date de publication:
15 Aug 2023
15 Aug 2023
Historique:
received:
06
07
2023
revised:
31
07
2023
accepted:
09
08
2023
medline:
26
8
2023
pubmed:
26
8
2023
entrez:
26
8
2023
Statut:
epublish
Résumé
Williams syndrome (WS) is a neurodevelopmental disorder characterized by distinctive cognitive and personality profiles which also impacts various physiological systems. The syndrome arises from the deletion of about 25 genes located on chromosome 7q11.23, including
Identifiants
pubmed: 37626769
pii: biomedicines11082273
doi: 10.3390/biomedicines11082273
pmc: PMC10452363
pii:
doi:
Types de publication
Journal Article
Langues
eng
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