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Brain. 2016 May;139(Pt 5):e28. doi: 10.1093/brain/aww033. Epub 2016 Mar 5.

NEK1 mutations in familial amyotrophic lateral sclerosis.

Author information

1
Neurology Department, Ulm University, Ulm, Germany.
2
Institute of Human Genetics, Helmholtz Zentrum München, Neuherberg, Germany.
3
Kantonsspital St. Gallen, Muskelzentrum / ALS Clinic, St. Gallen, Switzerland.
4
Institute of Human Genetics, Ulm University, Ulm, Germany.
5
Department of Neurology, Malmö University Hospital, Malmö, Sweden.
6
Institute of Human Genetics, Ulm University, Ulm, Germany Institute of Human Genetics, Medical Centre Hamburg-Eppendorf, Hamburg, Germany.
7
SyNergy, Munich Cluster for Systems Neurology, Ludwig Maximilians Universität München, Germany Institute of Human Genetics, Technische Universität München, München, Germany.
8
Neurology Department, Ulm University, Ulm, Germany Department of Pharmacology and Clinical Neurosience, Umeå University, Umeå, Sweden.
9
Neurology Department, Ulm University, Ulm, Germany jochen.weishaupt@uni-ulm.de.
PMID:
26945885
DOI:
10.1093/brain/aww033
[Indexed for MEDLINE]

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