Mutations in mitofusin 2 are a major cause for autosomal dominant axonal Charcot-Marie-Tooth neuropathy

被引：0
|
作者：
Claeys, K
Verhoeven, K
Züchner, S
Schröder, JM
Vance, JM
Timmerman, V
De Jonghe, P
机构：
[1] Univ Antwerp VIB, Dept Mol Genet, B-2020 Antwerp, Belgium
[2] Duke Univ, Med Ctr, Ctr Human Genet, Durham, NC USA
[3] Rhein Westfal TH Aachen, Univ Hosp, Dept Neuropathol, D-5100 Aachen, Germany
来源：
JOURNAL OF THE PERIPHERAL NERVOUS SYSTEM | 2005年 / 10卷
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中图分类号：
R74 [神经病学与精神病学];
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页码：16 / 17
页数：2
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