COCH-related autosomal dominant nonsyndromic hearing loss: a phenotype-genotype study.
Hum Genet
; 141(3-4): 889-901, 2022 Apr.
Article
in En
| MEDLINE
| ID: mdl-34529116
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Deafness
/
Hearing Loss
/
Hearing Loss, Sensorineural
Limits:
Humans
Language:
En
Journal:
Hum Genet
Year:
2022
Document type:
Article