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

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：

4112

引用

页数：3

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