Novel compound heterozygous mutations in MYO7A Associated with Usher syndrome 1 in a Chinese family.
PLoS One
; 9(7): e103415, 2014.
Article
in En
| MEDLINE
| ID: mdl-25080338
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Myosins
/
Usher Syndromes
/
Heterozygote
/
Mutation
Type of study:
Prognostic_studies
/
Risk_factors_studies
Limits:
Animals
/
Female
/
Humans
/
Male
/
Middle aged
Country/Region as subject:
Asia
Language:
En
Journal:
PLoS One
Journal subject:
CIENCIA
/
MEDICINA
Year:
2014
Type:
Article