OPA1 deletions account for 26% of cases with autosomal dominant optic atrophy (ADOA, Kjer disease)

被引：0
|
作者：
Zanlonghi, Xavier [1 ]
Lenaers, Guy [2 ]
Charif, Majida [3 ]
Barrucand, Anne [1 ]
Guichet, Agnes [2 ]
Reynier, Pascal [2 ]
Desquiret-Dumas, Valerie [2 ]
Amati-Bonneau, Patrizia [2 ]
机构：
[1] Ctr Hosp Univ Rennes, Rennes, Bretagne, France
[2] Univ Angers, Angers, France
[3] Genet & Immuno Cell Therapy Team, Oujda, Morocco
来源：
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE | 2023年 / 64卷 / 08期
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中图分类号：
R77 [眼科学];
学科分类号：
100212 ;
摘要：
4112
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页数：3
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