Phenotypic characterization of a Chinese family with autosomal dominant cone–rod dystrophy related to GUCY2D

被引：0
|
作者：
Fei Xu
Fangtian Dong
Hui Li
Xin Li
Ruxin Jiang
Ruifang Sui
机构：
[1] Peking Union Medical College and Chinese Academy of Medical Sciences,Department of Ophthalmology, Peking Union Medical College Hospital
[2] Chinese Academy of Sciences,Beijing Institute of Genomics
来源：
Documenta Ophthalmologica | 2013年 / 126卷
关键词：
Cone–rod dystrophy; Clinical phenotype; Follow-up; Mutation;
D O I：
暂无
中图分类号：
学科分类号：
摘要：
引用
收藏
页码：233 / 240
页数：7
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