CRX mutations in patients with phenotypes resembling Stargardt disease

被引：0
|
作者：
Xie, Yajing [1 ]
Tsang, Stephen H. [1 ,2 ]
Ayuso, Carmen [3 ]
Lee, Winston [1 ]
Jhangiani, Shalini N. [4 ]
Gambin, Tomasz [4 ]
Yuan, Bo [4 ]
Lupski, James R. [4 ]
Allikmets, Rando [1 ,2 ]
机构：
[1] Columbia Univ, Opthalmol, New York, NY USA
[2] Columbia Univ, Pathol & Cell Biol, New York, NY USA
[3] Univ Hosp Fdn Jimenez Diaz, Clin Genet, Madrid, Spain
[4] Baylor Coll Med, Mol & Human Genet, Houston, TX 77030 USA
来源：
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE | 2014年 / 55卷 / 13期
关键词：
539; genetics; 537 gene screening; 696 retinal degenerations: hereditary;
D O I：
暂无
中图分类号：
R77 [眼科学];
学科分类号：
100212 ;
摘要：
3256
引用
收藏
页数：2
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