Autosomal dominant optic neuropathy caused by pathogenic OPA1 mutation in Leber's hereditary optic neuropathy m.3460G>A mutation carriers: one family

被引：0

作者：

Catarino, C. ^{[1
]}

Von Livonius, B. ^{[2
]}

Hoertnagel, K. ^{[3
]}

Biskup, S. ^{[3
]}

Rudolph, G. ^{[2
]}

Priglinger, C. ^{[2
]}

Klopstock, T. ^{[1
]}

机构：

[1] Ludwig Maximilians Univ Munchen, Neurol, Friedrich Baur Inst, Munich, Germany

[2] Ludwig Maximilians Univ Munchen, Ophthalmol, Munich, Germany

[3] CeGaT GmbH, Tubingen, Germany

来源：

EUROPEAN JOURNAL OF NEUROLOGY | 2020年 / 27卷

关键词：

D O I：

暂无

中图分类号：

R74 [神经病学与精神病学];

学科分类号：

摘要：

EPR2174

引用

页码：367 / 367

页数：1

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Autosomal dominant optic neuropathy caused by pathogenic OPA1 mutation in Leber's hereditary optic neuropathy m.3460G&gt;A mutation carriers: one family

Autosomal dominant optic neuropathy caused by pathogenic OPA1 mutation in Leber's hereditary optic neuropathy m.3460G>A mutation carriers: one family