Different functional consequences of two missense mutations in the GJB2 gene associated with non-syndromic hearing loss.
Hum Mutat
; 30(7): E716-27, 2009 Jul.
Article
in En
| MEDLINE
| ID: mdl-19384972
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Connexins
/
Mutation, Missense
/
Hearing Loss
Type of study:
Risk_factors_studies
Limits:
Humans
Country/Region as subject:
Asia
Language:
En
Journal:
Hum Mutat
Journal subject:
GENETICA MEDICA
Year:
2009
Type:
Article
Affiliation country:
South Korea