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Mutations in XRCC1 cause cerebellar ataxia and peripheral neuropathy.

O'Connor, E; Vandrovcova, J; Bugiardini, E; Chelban, V; Manole, A; Davagnanam, I; Wiethoff, S; Pittman, A; Lynch, DS; Efthymiou, S; et al. O'Connor, E; Vandrovcova, J; Bugiardini, E; Chelban, V; Manole, A; Davagnanam, I; Wiethoff, S; Pittman, A; Lynch, DS; Efthymiou, S; Marino, S; Manzur, AY; Roberts, M; Hanna, MG; Houlden, H; Matthews, E; Wood, NW (2018) Mutations in XRCC1 cause cerebellar ataxia and peripheral neuropathy. J Neurol Neurosurg Psychiatry, 89 (11). pp. 1230-1232. ISSN 1468-330X https://doi.org/10.1136/jnnp-2017-317581
SGUL Authors: Pittman, Alan Michael

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Item Type: Article
Additional Information: © Article author(s) (or their employer(s) unless otherwise stated in the text of the article) 2018. All rights reserved. No commercial use is permitted unless otherwise expressly granted. This is an open access article distributed in accordance with the terms of the Creative Commons Attribution (CC BY 4.0) license, which permits others to distribute, remix, adapt and build upon this work, for commercial use, provided the original work is properly cited. See: http://creativecommons.org/licenses/by/4.0/
Keywords: cerebellar ataxia, cerebellar degeneration, genetics, neurogenetics, neuropathy, 11 Medical And Health Sciences, 17 Psychology And Cognitive Sciences, Neurology & Neurosurgery
SGUL Research Institute / Research Centre: Academic Structure > Molecular and Clinical Sciences Research Institute (MCS)
Journal or Publication Title: J Neurol Neurosurg Psychiatry
ISSN: 1468-330X
Language: eng
Dates:
DateEvent
November 2018Published
22 February 2018Published Online
24 January 2018Accepted
Publisher License: Creative Commons: Attribution 4.0
Projects:
Project IDFunderFunder ID
G-1107Parkinson's UKhttp://dx.doi.org/10.13039/501100000304
UNSPECIFIEDBrain Research Trusthttp://dx.doi.org/10.13039/501100000368
UNSPECIFIEDMedical Research Councilhttp://dx.doi.org/10.13039/501100000265
104033Wellcome Trusthttp://dx.doi.org/10.13039/100004440
2012D305121EU FP7/2007D2013UNSPECIFIED
UNSPECIFIEDMDA USAUNSPECIFIED
UNSPECIFIEDMuscular Dystrophy UKUNSPECIFIED
UNSPECIFIEDRosetrees Trusthttp://dx.doi.org/10.13039/501100000833
UNSPECIFIEDAtaxia UKhttp://dx.doi.org/10.13039/501100000346
UNSPECIFIEDBritish Neurological Surveillance UnitUNSPECIFIED
UNSPECIFIEDNational Institute for HealthUNSPECIFIED
PubMed ID: 29472272
Go to PubMed abstract
URI: https://openaccess.sgul.ac.uk/id/eprint/110757
Publisher's version: https://doi.org/10.1136/jnnp-2017-317581

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