Autosomal dominant cone–rod retinal dystrophy (CORD6) from heterozygous mutation of GUCY2D , which encodes retinal guanylate cyclase 1 1The authors have no proprietary interests in the materials mentioned in the study.-Reference-Cited by-同舟云学术

Autosomal dominant cone–rod retinal dystrophy (CORD6) from heterozygous mutation of GUCY2D , which encodes retinal guanylate cyclase 1 1The authors have no proprietary interests in the materials mentioned in the study.

Published:2000-01 Issue:1 Volume:107 Page:55-61
ISSN:0161-6420
Container-title:Ophthalmology
language:en
Short-container-title:Ophthalmology

Author:

Gregory-Evans Kevin,Kelsell Rosemary E,Gregory-Evans Cheryl Y,Downes Susan M,Fitzke Fred W,Holder Graham E,Simunovic Matthew,Mollon John D,Taylor Rachel,Hunt David M,Bird Alan C,Moore Anthony T

Publisher

Elsevier BV

Subject

Ophthalmology

Reference43 articles.

1. Progressive cone-rod degeneration;Berson;Arch Ophthalmol,1968

2. The cone dystrophies;Simunovic;Eye,1998

3. Cone-rod dystrophy due to mutations in a novel photoreceptor-specific homeobox gene (CRX) essential for maintenance of the photoreceptor;Freund;Cell,1997

4. Autosomal dominant cone-rod dystrophy associated with a Val200Glu mutation of the peripherin/rds gene;Nakazawa;Retina,1996

5. Autosomal dominant cone-rod dystrophy associated with mutations in codon 244 (Asn244His) and codon 184 (Tyr184Ser) of the peripherin/rds gene;Nakazawa;Arch Ophthalmol,1996

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