Follow Up of Families With Syndromic Autosomal Dominant Optic Atrophy (SADOA)

被引:0
作者
Crochet, M. [1 ]
Puech, B. [1 ]
Drumare, I. [1 ]
Bonneau, P. [2 ]
Lacour, A. [3 ]
Gabanou, F. [4 ]
Defoort, S. [1 ]
机构
[1] Hop Univ, Neuroophtalmol & Explorat Vis, Lille, France
[2] INSERM, U694, Angers, France
[3] Hop Univ, Dept Neurol, Lille, France
[4] Hop Univ, Dept ORL, Lille, France
关键词
visual impairment: neuro-ophthalmological disease; genetics; electrophysiology: clinical;
D O I
暂无
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
1002
引用
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页数:2
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