VCP mutations are not a major cause of familial amyotrophic lateral sclerosis in the UK

File(s)

VCP Manuscript revised DECEMBER2014.docx (476.18 KB)

Accepted version

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Author(s)

Kwok, CT

Wang, H-Y

Morris, AG

Smith, B

Shaw, C

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Type

Journal Article

Date Issued

2015-01-16

Date Acceptance

2015-01-13

Citation

Journal of the Neurological Sciences, 2015, 349 (1-2), pp.209-213

URI

http://hdl.handle.net/10044/1/21565

DOI

https://www.dx.doi.org/10.1016/j.jns.2015.01.021

ISSN

0022-510X

Publisher

Elsevier

Start Page

209

End Page

213

Journal / Book Title

Journal of the Neurological Sciences

Volume

349

Issue

1-2

Copyright Statement

Copyright © 2015 Elsevier Ltd. All rights reserved. NOTICE: this is the author’s version of a work that was accepted for publication in Journal of the Neurological Sciences. Changes resulting from the publishing process, such as peer review, editing, corrections, structural formatting, and other quality control mechanisms may not be reflected in this document. Changes may have been made to this work since it was submitted for publication. A definitive version was subsequently published in Journal of the Neurological Sciences, Volume 349, Issues 1–2, 16 jan 2015, DOI: 10.1016/j.jns.2015.01.021

License URL

http://www.rioxx.net/licenses/all-rights-reserved

Subjects

Science & Technology

Life Sciences & Biomedicine

Clinical Neurology

Neurosciences

Neurosciences & Neurology

Amyotrophic lateral sclerosis (ALS)

Familial ALS (FALS)

Valosin containing protein (VCP)

Inclusion body myopathy with Paget's disease of bone and fronto-temporal dementia (IBMPFD)

Frontotemporal dementia (FTD)

Paget's disease of bone (PDB)

Hexanucleotide repeat expansion

VALOSIN-CONTAINING-PROTEIN

INCLUSION-BODY MYOPATHY

FRONTOTEMPORAL LOBAR DEGENERATION

HEXANUCLEOTIDE REPEAT

ALS

TDP-43

INVOLVEMENT

EXPANSIONS

AUTOPHAGY

DEMENTIA

Publication Status

Published