Striking phenotypic variation in a family with the P506S UBQLN2 mutation including amyotrophic lateral sclerosis, spastic paraplegia, and frontotemporal dementia

Gkazi, S.A., Troakes, C., Topp, S. et al. (10 more authors) (2019) Striking phenotypic variation in a family with the P506S UBQLN2 mutation including amyotrophic lateral sclerosis, spastic paraplegia, and frontotemporal dementia. Neurobiology of Aging, 73. 229.e5-229.e9. ISSN 0197-4580

Abstract

Metadata

Authors/Creators:
Copyright, Publisher and Additional Information: © 2018 Elsevier.
Keywords: Familial amyotrophic lateral sclerosis (FALS); Spastic paraplegia (SP); Frontotemporal dementia (FTD); UBQLN2
Dates:
  • Accepted: 15 August 2018
  • Published (online): 24 August 2018
  • Published: 1 January 2019
Institution: The University of Sheffield
Academic Units: The University of Sheffield > Sheffield Teaching Hospitals
Depositing User: Symplectic Sheffield
Date Deposited: 03 Dec 2018 12:14
Last Modified: 03 Dec 2018 12:14
Published Version: https://doi.org/10.1016/j.neurobiolaging.2018.08.0...
Status: Published
Publisher: Elsevier
Refereed: Yes
Identification Number: https://doi.org/10.1016/j.neurobiolaging.2018.08.015
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