Mitochondrial ATP6 mutation m.9176T>C leading to mild late-onset manifestation of a neurologic multisystem disorder

被引：0
|
作者：
Stauber, J. [1 ]
Einhaeupl, M. [1 ]
Wagner, M. [2 ]
Roeber, S. [3 ]
Klopstock, T. [1 ]
机构：
[1] Friedrich Baur Inst, Munich, Germany
[2] Tech Univ Munich, Inst Human Genet, Munich, Germany
[3] LMU, Neuropathol, Munich, Germany
来源：
EUROPEAN JOURNAL OF NEUROLOGY | 2018年 / 25卷
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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：
EPR2133
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收藏
页码：453 / 453
页数：1
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