Novel Pathogenic Variants in the Gene Encoding Stereocilin (
DFNB16
STRC
genetic epidemiology
non-syndromic hearing impairment
stereocilin
Journal
Biomedicines
ISSN: 2227-9059
Titre abrégé: Biomedicines
Pays: Switzerland
ID NLM: 101691304
Informations de publication
Date de publication:
31 Oct 2023
31 Oct 2023
Historique:
received:
10
10
2023
revised:
24
10
2023
accepted:
27
10
2023
medline:
25
11
2023
pubmed:
25
11
2023
entrez:
25
11
2023
Statut:
epublish
Résumé
Non-syndromic hearing impairment (NSHI) is a very heterogeneous genetic condition, involving over 130 genes. Mutations in
Identifiants
pubmed: 38001944
pii: biomedicines11112943
doi: 10.3390/biomedicines11112943
pmc: PMC10668944
pii:
doi:
Types de publication
Journal Article
Langues
eng
Subventions
Organisme : NIMHD NIH HHS
ID : L60 MD003721
Pays : United States
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