Rhodopsin Thr58Arg Mutation in a Family with Autosomal Dominant Retinitis Pigmentosa-Reference-Cited by-同舟云学术

Rhodopsin Thr58Arg Mutation in a Family with Autosomal Dominant Retinitis Pigmentosa

Published:1991-12 Issue:12 Volume:98 Page:1797-1805
ISSN:0161-6420
Container-title:Ophthalmology
language:en
Short-container-title:Ophthalmology

Author:

Richards Julia E.,Kuo Chen-Yu,Boehnke Michael,Sieving Paul A.

Publisher

Elsevier BV

Subject

Ophthalmology

Reference26 articles.

1. Autosomal dominant retinitis pigmentosa (ADRP): localization of an ADRP gene to the long arm of chromosome 3;McWilliam;Genomics,1989

2. Linkage to D3S47 (C17) in one large autosomal dominant retinitis pigmentosa family and exclusion in another: confirmation of genetic heterogeneity;Lester;Am J Hum Genet.,1990

3. No evidence for linkage between late onset autosomal dominant retinitis pigmentosa and chromosome 3 locus D3S47 (C17): evidence for genetic heterogeneity;Inglehearn;Genomics,1990

4. Gene of type II autosomal dominant retinitis pigmentosa maps on the long arm of chromosome 3;Olsson;Am J H Med Genet,1990

5. Autosomal dominant retinitis pigmentosa: linkage to rhodospin and evidence for genetic heterogeneity;Farrar;Genomics,1990

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