Two novel mutations in conserved codons indicate that CHCHD10 is a gene associated with motor neuron disease

被引：90
作者：
Mueller, Kathrin [1 ]
Andersen, Peter M. [1 ,2 ,3 ]
Huebers, Annemarie [1 ]
Marroquin, Nicolai [1 ,4 ]
Volk, Alexander E. [4 ]
Danzer, Karin M. [1 ]
Meitinger, Thomas [5 ,6 ]
Ludolph, Albert C. [1 ,3 ]
Strom, Tim M. [5 ,6 ]
Weishaupt, Jochen H. [1 ]
机构：
[1] Univ Ulm, Dept Neurol, D-89081 Ulm, Germany
[2] Umea Univ, Dept Pharmacol & Clin Neurosci, Umea, Sweden
[3] Virtual Helmholtz Inst RNA Dysmetab Amyotrop Late, Berlin, Germany
[4] Univ Ulm, Inst Human Genet, D-89081 Ulm, Germany
[5] Helmholtz Zentrum Munchen, Inst Human Genet, Neuherberg, Germany
[6] Tech Univ Munich, Inst Human Genet, D-80290 Munich, Germany
来源：
BRAIN | 2014年 / 137卷
关键词：
AMYOTROPHIC-LATERAL-SCLEROSIS;
D O I：
10.1093/brain/awu227
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
页数：3
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