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

被引：91

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

页数：3

共 6 条

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