Oligogenic inheritance of optineurin (OPTN) andC9ORF72mutations in ALS highlights localisation of OPTN in the TDP-43-negative inclusions ofC9ORF72-ALS-Reference-Cited by-同舟云学术

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Oligogenic inheritance of optineurin (OPTN) andC9ORF72mutations in ALS highlights localisation of OPTN in the TDP-43-negative inclusions ofC9ORF72-ALS

Published:2015-08-24 Issue:2 Volume:36 Page:125-134
ISSN:0919-6544
Container-title:Neuropathology
language:en
Short-container-title:Neuropathology

Author:

Bury Joanna J.¹,Highley J. Robin¹,Cooper-Knock Johnathan¹,Goodall Emily F.¹,Higginbottom Adrian¹,McDermott Christopher J.¹,Ince Paul G.¹,Shaw Pamela J.¹,Kirby Janine¹

Affiliation:

1. Sheffield Institute for Translational Neuroscience (SITraN), Department of Neuroscience; University of Sheffield; Sheffield UK

Funder

Medical Research Council

Seventh Framework Programme

Motor Neurone Disease Association

National Institute for Health Research

Publisher

Wiley

Subject

Clinical Neurology,General Medicine,Pathology and Forensic Medicine

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/neup.12240/fullpdf

Reference53 articles.

1. Diagnosis and management of motor neurone disease;McDermott;BMJ,2008

2. Global epidemiology of amyotrophic lateral sclerosis: a systematic review of the published literature;Chio;Neuroepidemiology,2013

3. Effects of gender in amyotrophic lateral sclerosis;McCombe;Gend Med,2010

4. Rate of familial amyotrophic lateral sclerosis: a systematic review and meta-analysis;Byrne;J Neurol Neurosurg Psychiatry,2011

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