Oligogenic inheritance of optineurin (OPTN) and C9ORF72 mutations in ALS highlights localisation of OPTN in the TDP-43-negative inclusions of C9ORF72-ALS.

Bury, J.J., Highley, J.R., Cooper-Knock, J. et al. (6 more authors) (2016) Oligogenic inheritance of optineurin (OPTN) and C9ORF72 mutations in ALS highlights localisation of OPTN in the TDP-43-negative inclusions of C9ORF72-ALS. Neuropathology , 36 (2). pp. 125-134. ISSN 0919-6544

Abstract

Metadata

Authors/Creators:
  • Bury, J.J.
  • Highley, J.R.
  • Cooper-Knock, J.
  • Goodall, E.F.
  • Higginbottom, A.
  • McDermott, C.J.
  • Ince, P.G.
  • Shaw, P.J.
  • Kirby, J.
Copyright, Publisher and Additional Information: © 2015 Japanese Society of Neuropathology. This is an author produced version of a paper subsequently published in Neuropathology. Uploaded in accordance with the publisher's self-archiving policy.
Keywords: C9ORF72; amyotrophic lateral sclerosis; inclusion bodies; multifactorial inheritance; optineurin
Dates:
  • Accepted: 25 July 2015
  • Published (online): 24 August 2015
  • Published: April 2016
Institution: The University of Sheffield
Academic Units: The University of Sheffield > Faculty of Medicine, Dentistry and Health (Sheffield) > School of Medicine (Sheffield) > Department of Neuroscience (Sheffield)
Depositing User: Symplectic Sheffield
Date Deposited: 04 Nov 2015 17:37
Last Modified: 03 Apr 2019 11:12
Published Version: https://dx.doi.org/10.1111/neup.12240
Status: Published
Publisher: Wiley
Refereed: Yes
Identification Number: https://doi.org/10.1111/neup.12240
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