NEK1 mutations in familial amyotrophic lateral sclerosis.
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Brenner D
Neurology Department, Ulm University, Ulm, Germany.
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Müller K
Neurology Department, Ulm University, Ulm, Germany.
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Wieland T
Institute of Human Genetics, Helmholtz Zentrum München, Neuherberg, Germany.
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Weydt P
Neurology Department, Ulm University, Ulm, Germany.
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Böhm S
Neurology Department, Ulm University, Ulm, Germany.
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Lulé D
Neurology Department, Ulm University, Ulm, Germany.
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Hübers A
Neurology Department, Ulm University, Ulm, Germany.
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Neuwirth C
Kantonsspital St. Gallen, Muskelzentrum / ALS Clinic, St. Gallen, Switzerland.
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Weber M
Kantonsspital St. Gallen, Muskelzentrum / ALS Clinic, St. Gallen, Switzerland.
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Borck G
Institute of Human Genetics, Ulm University, Ulm, Germany.
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Wahlqvist M
Department of Neurology, Malmö University Hospital, Malmö, Sweden.
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Danzer KM
Neurology Department, Ulm University, Ulm, Germany.
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Volk AE
Institute of Human Genetics, Ulm University, Ulm, Germany Institute of Human Genetics, Medical Centre Hamburg-Eppendorf, Hamburg, Germany.
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Meitinger T
SyNergy, Munich Cluster for Systems Neurology, Ludwig Maximilians Universität München, Germany Institute of Human Genetics, Technische Universität München, München, Germany.
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Strom TM
SyNergy, Munich Cluster for Systems Neurology, Ludwig Maximilians Universität München, Germany Institute of Human Genetics, Technische Universität München, München, Germany.
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Otto M
Neurology Department, Ulm University, Ulm, Germany.
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Kassubek J
Neurology Department, Ulm University, Ulm, Germany.
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Ludolph AC
Neurology Department, Ulm University, Ulm, Germany.
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Andersen PM
Neurology Department, Ulm University, Ulm, Germany Department of Pharmacology and Clinical Neurosience, Umeå University, Umeå, Sweden.
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Weishaupt JH
Neurology Department, Ulm University, Ulm, Germany jochen.weishaupt@uni-ulm.de.
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Published in:
- Brain : a journal of neurology. - 2016
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Language
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Open access status
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bronze
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Identifiers
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Persistent URL
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https://sonar.ch/global/documents/559
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