SMARCA4 mutation causes human otosclerosis and a similar phenotype in mice.
J Med Genet
; 61(2): 117-124, 2024 Jan 19.
Article
in En
| MEDLINE
| ID: mdl-37399313
Full text:
1
Database:
MEDLINE
Main subject:
Otosclerosis
/
Hearing Loss
Type of study:
Etiology_studies
Limits:
Adult
/
Animals
/
Humans
Language:
En
Journal:
J Med Genet
Year:
2024
Type:
Article
Affiliation country:
Israel