NCOA3 identified as a new candidate to explain autosomal dominant progressive hearing loss.
Hum Mol Genet
; 29(22): 3691-3705, 2021 01 21.
Article
in En
| MEDLINE
| ID: mdl-33326993
Full text:
1
Database:
MEDLINE
Main subject:
Genetic Predisposition to Disease
/
Deafness
/
Nuclear Receptor Coactivator 3
/
Hearing Loss, Sensorineural
Type of study:
Prognostic_studies
Limits:
Adult
/
Animals
/
Humans
/
Male
Language:
En
Journal:
Hum Mol Genet
Journal subject:
BIOLOGIA MOLECULAR
/
GENETICA MEDICA
Year:
2021
Type:
Article
Affiliation country:
Brazil