Phenotype of autosomal dominant cone–rod dystrophy due to the R838C mutation of the GUCY2D gene encoding retinal guanylate cyclase-1

被引：0
|
作者：
M Smith
N Whittock
A Searle
M Croft
C Brewer
M Cole
机构：
[1] Torbay Hospital,Department of Ophthalmology
[2] Institute of Biomedical and Clinical Science,Department of Clinical Genetics
[3] Peninsula Medical School,undefined
[4] Royal Devon and Exeter Hospital,undefined
来源：
Eye | 2007年 / 21卷
关键词：
cone dystrophy; cone–rod dystrophy; GUCY2D; RETGC-1;
D O I：
暂无
中图分类号：
学科分类号：
摘要：
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页码：1220 / 1225
页数：5
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