Phenotype in homozygous and heterozygous carriers of BEST1 mutations in autosomal recessive Bestrophinopathy

被引：0
|
作者：
El Matri, K. [1 ,2 ]
Falfoul, Y. [1 ,2 ]
Habibi, I. [3 ]
Turki, A. [2 ]
Chebil, A. [1 ,2 ]
Schorderet, D. [3 ]
El Matri, L. [1 ,2 ]
机构：
[1] Hedi Rais Inst Ophthalmol, Ophtalmol, Tunis, Tunisia
[2] Oculogenet Lab, LR14SP01, Tunis, Tunisia
[3] Inst Res Ophthalmol, Sion, Switzerland
来源：
ACTA OPHTHALMOLOGICA | 2018年 / 96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：
F118
引用
收藏
页码：35 / 35
页数：1
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