Whole genome sequencing delineates novel non-coding variants and candidate genes in inherited retinal diseases

被引：0
|
作者：
Valero, Marta [1 ]
Bauwens, Miriam [1 ]
De Bruyne, Marieke [1 ]
Van den Broeck, Filip [2 ,3 ]
Dulst, Stephanie [1 ]
Quinten, Quinten [1 ]
Meunier, Audrey [4 ]
de Ravel, Thomy [5 ]
Ruys, Joke [6 ]
Van Heetvelde, Mattias [1 ]
Balikova, Irina [7 ]
Vermeer, Sascha [7 ]
De Zaeytijd, Julie [2 ,3 ]
Leroy, Bart [2 ,3 ,8 ,9 ]
De Baere, Elfride [1 ]
机构：
[1] Ghent Univ Hosp, Dept Biomol Med, Ctr Med Genet, Ghent, Belgium
[2] Ghent Univ Hosp, Dept Ophthalmol, Ghent, Belgium
[3] Ghent Univ Hosp, Dept Head & Skin, Ghent, Belgium
[4] ULB, Dept Ophthalmol, Univ Hosp St Pierre, Brussels, Belgium
[5] Univ Hosp Brussels, Ctr Med Genet, Brussels, Belgium
[6] ZNA Middelheim, Dept Ophthalmol, Antwerp, Belgium
[7] Univ Hosp Leuven, Dept Ophthalmol, Leuven, Belgium
[8] Childrens Hosp Philadelphia, Div Ophthalmol, Philadelphia, PA USA
[9] Childrens Hosp Philadelphia, Ctr Cellular & Mol Therapeut, Philadelphia, PA USA
来源：
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE | 2023年 / 64卷 / 08期
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：
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页数：4
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