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

页码：CP14 / CP17

页数：4

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