Mutations in SPG7 as an important cause of spastic-ataxia in a large british cohort: Hybrid phenotype helps direct screening

Metadata

Item Type:	Proceedings Paper
Authors/Creators:	Hewamadduma, C.A. Omalley, R. Robinson, M. Beauchamp, N. Rogers, T. Martindale, J. Mcdermott, C. https://orcid.org/0000-0002-1269-9053 Shaw, P. https://orcid.org/0000-0002-8925-2567 Hoggard, N. https://orcid.org/0000-0002-6447-7639 Hadjivassiliou, M. https://orcid.org/0000-0003-2542-8954
Copyright, Publisher and Additional Information:	© 2017 Elsevier. This is an author produced version of a paper subsequently published in Journal of the Neurological Sciences. Uploaded in accordance with the publisher's self-archiving policy. Article available under the terms of the CC-BY-NC-ND licence (https://creativecommons.org/licenses/by-nc-nd/4.0/)
Dates:	Published: 15 October 2017 Published (online): 1 December 2017
Institution:	The University of Sheffield
Academic Units:	The University of Sheffield > Sheffield Teaching Hospitals
Depositing User:	Symplectic Sheffield
Date Deposited:	19 Apr 2018 13:14
Last Modified:	01 Dec 2018 01:39
Published Version:	https://doi.org/10.1016/j.jns.2017.08.864
Status:	Published
Publisher:	Elsevier
Identification Number:	10.1016/j.jns.2017.08.864
Related URLs:	Author
Open Archives Initiative ID (OAI ID):	oai:eprints.whiterose.ac.uk:129741

CORE (COnnecting REpositories)