Coding and non-coding structural variants of ABCA4 contribute to the missing heritability in Stargardt disease, a prevalent inherited retinal disease

被引：0
|
作者：
Bauwens, M. [1 ]
Naessens, S. [1 ]
Van Cauwenbergh, C. [1 ,2 ,3 ]
Van Laethem, T. [1 ]
De Jaegere, S. [1 ]
Balikova, I. [2 ,3 ]
Sznajer, Y. [4 ]
De Zaeytijd, J. [2 ,3 ]
Leroy, B. P. [2 ,3 ,5 ,6 ]
De Baere, E. [1 ]
机构：
[1] Univ Ghent, Ctr Med Genet Ghent, Ghent, Belgium
[2] Univ Ghent, Dept Ophthalmol, Ghent, Belgium
[3] Ghent Univ Hosp, Ghent, Belgium
[4] Catholic Univ Louvain, Clin Univ St Luc, Ctr Genet Humaine, Brussels, Belgium
[5] Childrens Hosp Philadelphia, Div Ophthalmol, Philadelphia, PA 19104 USA
[6] Childrens Hosp Philadelphia, Ctr Cellular & Mol Therapeut, Philadelphia, PA 19104 USA
来源：
EUROPEAN JOURNAL OF HUMAN GENETICS | 2019年 / 27卷
关键词：
D O I：
暂无
中图分类号：
Q5 [生物化学]; Q7 [分子生物学];
学科分类号：
071010 ; 081704 ;
摘要：
P02.02A
引用
收藏
页码：42 / 43
页数：2
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