Genotyping strategy for congenital stationary night blindness (CSNB): conclusion from a comprehensive study and meta-analysis

被引：0
|
作者：
Zeitz, Christina [1 ]
Audo, Isabelle [1 ,2 ]
机构：
[1] Univ Pierre & Marie Curie Paris 6, CNRS, Inst Vis, INSERM,UMR S968,UMR 7210, Paris, France
[2] CHNO, INSERM, DHOS, CIC 503, Paris, France
来源：
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE | 2014年 / 55卷 / 13期
关键词：
563 inner retina dysfunction: hereditary; 537 gene screening; 604; mutations;
D O I：
暂无
中图分类号：
R77 [眼科学];
学科分类号：
100212 ;
摘要：
404
引用
收藏
页数：2
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