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

Hewamadduma, C.A., Omalley, R., Robinson, M. et al. (7 more authors) (2017) Mutations in SPG7 as an important cause of spastic-ataxia in a large british cohort: Hybrid phenotype helps direct screening. In: Journal of the Neurological Sciences. World Congress of Neurology (WCN 2017), 16-21 Sep 2017, Kyoto, Japan. Elsevier , pp. 304-305.

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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 (online): 1 December 2017
  • Published: 15 October 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: https://doi.org/10.1016/j.jns.2017.08.864
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