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The Newcastle University research output collection, currently available on ePrints, will shortly be moving to a new open repository platform, Figshare. To prepare for the data migration we have paused adding new content to ePrints, and will resume once the new repository is launched. During this time you will continue to have access to ePrints (but no new content will appear). We will share updates here when available.

Frequency of rare recessive mutations in unexplained late onset cerebellar ataxia

Lookup NU author(s): Dr Michael Keogh, Dr Hannah Steele, Dr Konstantinos Douroudis, Dr Angela Pyle, Dr Jennifer Duff, Raf HussainORCiD, Tania Smertenko, Dr Helen GriffinORCiD, Dr Mauro Santibanez Koref, Professor Rita HorvathORCiD, Professor Patrick Chinnery

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Publication metadata

Author(s): Keogh MJ, Steele H, Douroudis K, Pyle A, Duff J, Hussain R, Smertenko T, Griffin H, Santibanez-Koref M, Horvath R, Chinnery PF

Publication type: Article

Publication status: Published

Journal: Journal of Neurology

Year: 2015

Volume: 262

Issue: 8

Pages: 1822-1827

Print publication date: 01/08/2015

Online publication date: 16/05/2015

Acceptance date: 29/04/2015

Date deposited: 06/07/2015

ISSN (print): 0340-5354

ISSN (electronic): 1432-1459

Publisher: Springer

URL: http://dx.doi.org/10.1007/s00415-015-7772-x

DOI: 10.1007/s00415-015-7772-x

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Funding

Funder referenceFunder name
Newcastle University
EU FP7 TIRCON
National Institute for Health Research (NIHR) Newcastle Biomedical Research Centre based at Newcastle upon Tyne Hospitals NHS Foundation Trust
096919Z/11/ZWellcome Trust Centre for Mitochondrial Research
309548European Research Council
G1000848Medical Research Council (UK)
G0601943Medical Research Council (UK) Centre for Translational Muscle Disease research

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