NEK1mutations in familial amyotrophic lateral sclerosis-Reference-Cited by-同舟云学术

NEK1mutations in familial amyotrophic lateral sclerosis

Published:2016-03-05 Issue:5 Volume:139 Page:e28-e28
ISSN:0006-8950
Container-title:Brain
language:en
Short-container-title:Brain

Author:

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

Publisher

Oxford University Press (OUP)

Subject

Clinical Neurology

Link

http://academic.oup.com/brain/article-pdf/139/5/e28/7484129/aww033.pdf

Reference9 articles.

1. EFNS guidelines on the Clinical Management of Amyotrophic Lateral Sclerosis (MALS) – revised report of an EFNS task force

2. A mitochondrial origin for frontotemporal dementia and amyotrophic lateral sclerosis through CHCHD10 involvement

3. Exome sequencing in amyotrophic lateral sclerosis identifies risk genes and pathways

4. Dysfunctional nitric oxide signalling increases risk of myocardial infarction

5. Haploinsufficiency of TBK1 causes familial ALS and fronto-temporal dementia

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