NEK1 mutations in familial amyotrophic lateral sclerosis

被引：101
作者：
Brenner, David [1 ]
Mueller, Kathrin [1 ]
Wieland, Thomas [2 ]
Weydt, Patrick [1 ]
Boehm, Sarah [1 ]
Lule, Dorothee [1 ]
Huebers, Annemarie [1 ]
Neuwirth, Christoph [3 ]
Weber, Markus [3 ]
Borck, Guntram [4 ]
Wahlqvist, Magnus [5 ]
Danzer, Karin M. [1 ]
Volk, Alexander E. [4 ,6 ]
Meitinger, Thomas [7 ,8 ]
Strom, Tim M. [7 ,8 ]
Otto, Markus [1 ]
Kassubek, Jan [1 ]
Ludolph, Albert C. [1 ]
Andersen, Peter M. [1 ,9 ]
Weishaupt, Jochen H. [1 ]
机构：
[1] Univ Ulm, Dept Neurol, Albert Einstein Allee 11, D-89081 Ulm, Germany
[2] Helmholtz Zentrum Munchen, Inst Human Genet, Neuherberg, Germany
[3] Kantonsspital, Muskelzentrum, ALS Clin, St Gallen, Switzerland
[4] Univ Ulm, Inst Human Genet, Albert Einstein Allee 11, D-89081 Ulm, Germany
[5] Malmo Univ Hosp, Dept Neurol, Malmo, Sweden
[6] Med Ctr Hamburg Eppendorf, Inst Human Genet, Hamburg, Germany
[7] Univ Munich, Munich Cluster Syst Neurol, SyNergy, Marchioninistr 15, D-81377 Munich, Germany
[8] Tech Univ Munich, Inst Human Genet, D-80290 Munich, Germany
[9] Umea Univ, Dept Pharmacol & Clin Neurosi, Umea, Sweden
来源：
BRAIN | 2016年 / 139卷
关键词：
FRONTOTEMPORAL DEMENTIA; RISK;
D O I：
10.1093/brain/aww033
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：CP14 / CP17
页数：4
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