[A Chinese family with autosomal dominant retinitis pigmentosa and a pro347Leu rhodopsin gene mutation]
Chin Med J (Engl)
.
2000 Jun;113(6):574-6.
[Article in Chinese]
Authors
H Yang
1
,
C Luo
,
J Zhou
,
M Yan
Affiliation
1
Department of Ophthalmology, Shanghai First People's Hospital, Shanghai 200080, China.
PMID:
11775885
No abstract available
Publication types
Case Reports
Research Support, Non-U.S. Gov't
MeSH terms
Adult
Codon*
Female
Humans
Male
Middle Aged
Mutation*
Pedigree
Retinitis Pigmentosa / genetics*
Rhodopsin / genetics*
Substances
Codon
Rhodopsin