Novel, pathogenic insertion variant of GSDME associates with autosomal dominant hearing loss in a large Chinese pedigree.
J Cell Mol Med
; 28(1): e18004, 2024 01.
Article
in En
| MEDLINE
| ID: mdl-37864300
Key words
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Deafness
/
Hearing Loss
/
Hearing Loss, Sensorineural
Limits:
Humans
Country/Region as subject:
Asia
Language:
En
Journal:
J Cell Mol Med
Journal subject:
BIOLOGIA MOLECULAR
Year:
2024
Document type:
Article
Affiliation country:
Country of publication: