NEK1 mutations in familial amyotrophic lateral sclerosis

David Brenner; Kathrin Müller; Thomas Wieland; Patrick Weydt; Sarah Böhm; Dorothee Lule; Annemarie Hübers; Christoph Neuwirth; Markus Weber; Guntram Borck; Magnus Wahlqvist; Karin M. Danzer; Alexander E. Volk; Thomas Meitinger; Tim M. Strom; Markus Otto; Jan Kassubek; Albert C. Ludolph; Peter M. Andersen; Jochen H. Weishaupt

doi:10.1093/brain/aww033

NEK1 mutations in familial amyotrophic lateral sclerosis

David Brenner, Kathrin Müller, Thomas Wieland, Patrick Weydt, Sarah Böhm, Dorothee Lule, Annemarie Hübers, Christoph Neuwirth, Markus Weber, Guntram Borck, Magnus Wahlqvist, Karin M. Danzer, Alexander E. Volk, Thomas Meitinger, Tim M. Strom, Markus Otto, Jan Kassubek, Albert C. Ludolph, Peter M. Andersen, Jochen H. Weishaupt

Medicine and Health

Research output: Contribution to journal › Letter › peer-review

108 Scopus citations

Original language	English
Pages (from-to)	e28
Journal	Brain
Volume	139
Issue number	5
DOIs	https://doi.org/10.1093/brain/aww033
State	Published - 1 May 2016

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Brenner, D., Müller, K., Wieland, T., Weydt, P., Böhm, S., Lule, D., Hübers, A., Neuwirth, C., Weber, M., Borck, G., Wahlqvist, M., Danzer, K. M., Volk, A. E., Meitinger, T., Strom, T. M., Otto, M., Kassubek, J., Ludolph, A. C., Andersen, P. M., & Weishaupt, J. H. (2016). NEK1 mutations in familial amyotrophic lateral sclerosis. Brain, 139(5), e28. https://doi.org/10.1093/brain/aww033

@article{0194b85d37df4091af1067d447797861,

title = "NEK1 mutations in familial amyotrophic lateral sclerosis",

author = "David Brenner and Kathrin M{\"u}ller and Thomas Wieland and Patrick Weydt and Sarah B{\"o}hm and Dorothee Lule and Annemarie H{\"u}bers and Christoph Neuwirth and Markus Weber and Guntram Borck and Magnus Wahlqvist and Danzer, {Karin M.} and Volk, {Alexander E.} and Thomas Meitinger and Strom, {Tim M.} and Markus Otto and Jan Kassubek and Ludolph, {Albert C.} and Andersen, {Peter M.} and Weishaupt, {Jochen H.}",

note = "Funding Information: This work was supported in whole or in parts by a grant from the German Federal Ministry of Education and Research (JPND {"}STRENGTH{"} consortium; German network for ALS research MND-NET), the Charcot Foundation for ALS Research, the virtual Helmholtz Institute {"}RNA-Dysmetabolismus in ALS and FTD{"} and the DFG-funded Swabian ALS Registry, the Swedish Brain Foundation, the Swedish Research Council and the Knut and Alice Wallenberg Foundation.",

year = "2016",

month = may,

day = "1",

doi = "10.1093/brain/aww033",

language = "English",

volume = "139",

pages = "e28",

journal = "Brain",

issn = "0006-8950",

publisher = "Oxford University Press",

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Brenner, D, Müller, K, Wieland, T, Weydt, P, Böhm, S, Lule, D, Hübers, A, Neuwirth, C, Weber, M, Borck, G, Wahlqvist, M, Danzer, KM, Volk, AE, Meitinger, T, Strom, TM, Otto, M, Kassubek, J, Ludolph, AC, Andersen, PM & Weishaupt, JH 2016, 'NEK1 mutations in familial amyotrophic lateral sclerosis', Brain, vol. 139, no. 5, pp. e28. https://doi.org/10.1093/brain/aww033

TY - JOUR

T1 - NEK1 mutations in familial amyotrophic lateral sclerosis

AU - Brenner, David

AU - Müller, Kathrin

AU - Wieland, Thomas

AU - Weydt, Patrick

AU - Böhm, Sarah

AU - Lule, Dorothee

AU - Hübers, Annemarie

AU - Neuwirth, Christoph

AU - Weber, Markus

AU - Borck, Guntram

AU - Wahlqvist, Magnus

AU - Danzer, Karin M.

AU - Volk, Alexander E.

AU - Meitinger, Thomas

AU - Strom, Tim M.

AU - Otto, Markus

AU - Kassubek, Jan

AU - Ludolph, Albert C.

AU - Andersen, Peter M.

AU - Weishaupt, Jochen H.

N1 - Funding Information: This work was supported in whole or in parts by a grant from the German Federal Ministry of Education and Research (JPND "STRENGTH" consortium; German network for ALS research MND-NET), the Charcot Foundation for ALS Research, the virtual Helmholtz Institute "RNA-Dysmetabolismus in ALS and FTD" and the DFG-funded Swabian ALS Registry, the Swedish Brain Foundation, the Swedish Research Council and the Knut and Alice Wallenberg Foundation.

PY - 2016/5/1

Y1 - 2016/5/1

UR - http://www.scopus.com/inward/record.url?scp=84966477966&partnerID=8YFLogxK

U2 - 10.1093/brain/aww033

DO - 10.1093/brain/aww033

M3 - Letter

C2 - 26945885

AN - SCOPUS:84966477966

SN - 0006-8950

VL - 139

SP - e28

JO - Brain

JF - Brain

IS - 5

ER -

NEK1 mutations in familial amyotrophic lateral sclerosis

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