Two novel mutations in PRPF3 causing autosomal dominant retinitis pigmentosa.
Sci Rep
; 6: 37840, 2016 11 25.
Article
in En
| MEDLINE
| ID: mdl-27886254
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Nuclear Proteins
/
Retinitis Pigmentosa
/
Ribonucleoprotein, U4-U6 Small Nuclear
/
Polymorphism, Single Nucleotide
/
Asian People
Type of study:
Prognostic_studies
Limits:
Adolescent
/
Adult
/
Child
/
Child, preschool
/
Female
/
Humans
/
Male
Language:
En
Journal:
Sci Rep
Year:
2016
Document type:
Article
Affiliation country:
China
Country of publication:
United kingdom