Monogenic inheritance of Leber congenital amaurosis:: causation by a novel mutation in CRB1.

被引：0
|
作者：
Abouzeid, H
Dharmaraj, S
Sundin, O
Maumenee, I
机构：
[1] Johns Hopkins Univ, John Hopkins Ctr Hereditary Eye Dis, Baltimore, MD USA
[2] Johns Hopkins Univ, Lab Dev Genet, Baltimore, MD USA
[3] Univ Lausanne, Jules Gonin Eye Hosp, Lausanne, Switzerland
来源：
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE | 2004年 / 45卷
关键词：
D O I：
暂无
中图分类号：
R77 [眼科学];
学科分类号：
100212 ;
摘要：
4730
引用
收藏
页码：U510 / U510
页数：1
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