Diagnosis of spinal xanthomatosis by next-generation sequencing: identifying a rare, treatable mimic of hereditary spastic paraparesis.

Nicholls, Z., Hobson, E., Martindale, J.A. et al. (1 more author) (2015) Diagnosis of spinal xanthomatosis by next-generation sequencing: identifying a rare, treatable mimic of hereditary spastic paraparesis. Practical Neurology, 15 (4). pp. 280-283. ISSN 1474-7758

Abstract

Metadata

Authors/Creators:
  • Nicholls, Z.
  • Hobson, E.
  • Martindale, J.A.
  • Shaw, P.J.
Copyright, Publisher and Additional Information: © 2016 by the BMJ Publishing Group Ltd. This is an author produced version of a paper subsequently published in Practical Neurology. Uploaded in accordance with the publisher's self-archiving policy.
Keywords: Genetics; hereditary spastic paraplegia; metabolic disease; neurogenetics; spasticity
Dates:
  • Published: 1 August 2015
  • Accepted: 10 March 2015
Institution: The University of Sheffield
Academic Units: The University of Sheffield > Faculty of Medicine, Dentistry and Health (Sheffield) > School of Medicine (Sheffield)
The University of Sheffield > Sheffield Teaching Hospitals
Funding Information:
FunderGrant number
NATIONAL INSTITUTE FOR HEALTH RESEARCHUNSPECIFIED
Depositing User: Symplectic Sheffield
Date Deposited: 22 Jan 2016 16:06
Last Modified: 01 Jul 2017 15:13
Published Version: http://dx.doi.org/10.1136/practneurol-2015-001117
Status: Published
Publisher: BMJ Publishing Group
Refereed: Yes
Identification Number: https://doi.org/10.1136/practneurol-2015-001117
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