Mitochondrial DNA mutation 14487T>C manifesting as Leber's hereditary optic neuropathy

被引：9
|
作者：
Eckenweiler, M. [1 ]
Catarino, C. B. [2 ]
Gallenmueller, C. [2 ]
Klopstock, T. [2 ]
Lagreze, W. A. [3 ]
Korinthenberg, R. [1 ]
Kirschner, J. [1 ]
机构：
[1] Univ Ctr Pediat Freiburg, Dept Neuropediat & Muscle Disorders, D-79106 Freiburg, Germany
[2] Klinikum Univ Munchen, Neurol Klin, Friedrich Baur Inst, Munich, Germany
[3] Univ Freiburg, Med Ctr, Ctr Eye, Freiburg, Germany
来源：
JOURNAL OF NEUROLOGY | 2015年 / 262卷 / 12期
关键词：
LEIGH-SYNDROME; MTDNA MUTATIONS; M.14487T-GREATER-THAN-C; EPILEPSY; GENE;
D O I：
10.1007/s00415-015-7955-5
中图分类号：
R74 [神经病学与精神病学];
学科分类号：
摘要：
引用
收藏
页码：2776 / 2779
页数：4
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