Whole exome sequencing reveals CEP78 as a novel disease gene for cone-rod dystrophy

被引：0
|
作者：
Nikopoulos, Konstantinos [1 ]
Farinelli, Pietro [1 ]
Royer-Bertrand, Beryl [1 ]
Bedoni, Nicola [1 ]
Kjellstrom, Ulrika [2 ]
Andreasson, Sten [2 ]
Tsilimbaris, Miltiadis K. [3 ]
Tsika, Chrysanthi [3 ]
Blazaki, Stella [3 ]
Rivolta, Carlo [1 ]
机构：
[1] Univ Lausanne, Dept Med Genet, Lausanne, Switzerland
[2] Lund Univ, Dept Ophthalmol, Lund, Sweden
[3] Univ Crete, Sch Med, Dept Ophthalmol, Iraklion, Greece
来源：
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE | 2016年 / 57卷 / 12期
基金：
瑞士国家科学基金会;
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：
引用
收藏
页数：3
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