Macular Dystrophy Associated with Mutations at Codon 172 in the Human Retinal Degeneration Slow Gene-Reference-Cited by-同舟云学术

Macular Dystrophy Associated with Mutations at Codon 172 in the Human Retinal Degeneration Slow Gene

Published:1994-01 Issue:1 Volume:101 Page:12-22
ISSN:0161-6420
Container-title:Ophthalmology
language:en
Short-container-title:Ophthalmology

Author:

Wroblewski John J.,Wells John A.,Eckstein Anja,Fitzke Fred,Jubb Chris,Keen T. Jeffrey,Inglehearn Chris,Bhattacharya Shomi,Arden Geoffrey B.,Jay Marcelle,Bird Alan C.

Publisher

Elsevier BV

Subject

Ophthalmology

Reference29 articles.

1. Mutations within the rhodopsin gene in patients with autosomal dominant retinitis pigmentosa;Dryja;N Engl J Med,1990

2. Rhodopsin mutations in autosomal dominant retinitis pigmentosa;Sung;Proc Natl Acad Sci USA,1991

3. Autosomal dominant retinitis pigmentosa: four new mutations in rhodopsin, one of them in the retinal attachment site;Keen;Genomics,1991

4. A completed screen for mutations of the rhodopsin gene in a panel of patients with autosomal dominant retinitis pigmentosa;Inglehearn;Hum Mol Genet,1992

5. A three-base-pair deletion in the peripherin-rds gene in one form of retinitis pigmentosa;Farrar;Nature,1991

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