Five novel missense mutations of the rhodopsin gene in autosomal dominant retinitis pigmentosa
Hum Mol Genet
.
1994 Aug;3(8):1433-4.
doi: 10.1093/hmg/3.8.1433.
Authors
E Souied
1
,
S Gerber
,
J M Rozet
,
D Bonneau
,
J L Dufier
,
I Ghazi
,
N Philip
,
G Soubrane
,
G Coscas
,
A Munnich
, et al.
Affiliation
1
Service de Génétique, INSERM U-393, Hôpital des Enfants-Malades, Paris, France.
PMID:
7987331
DOI:
10.1093/hmg/3.8.1433
No abstract available
Publication types
Research Support, Non-U.S. Gov't
MeSH terms
Codon
Genes, Dominant
Genotype
Humans
Point Mutation*
Polymorphism, Single-Stranded Conformational
Retinitis Pigmentosa / genetics*
Rhodopsin / genetics*
Substances
Codon
Rhodopsin