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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.

Reply: Mutations in the CHCHD10 gene are a common cause of familial amyotrophic lateral sclerosis

Lookup NU author(s): David Moore, Dr Patrick Yu Wai Man

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Author(s): Bannwarth S, Ait-El-Mkadem S, Chaussenot A, Genin EC, Lacas-Gervais S, Fragaki K, Berg-Alonso L, Kageyama Y, Serre V, Moore D, Verschueren A, Rouzier C, Le Ber I, Auge G, Cochaud C, Lespinasse F, N'Guyen K, de Septenville A, Brice A, Yu-Wai-Man P, Sesaki H, Pouget J, Paquis-Flucklinger V

Publication type: Letter

Publication status: Published

Journal: Brain

Year: 2014

Volume: 137

Pages: 1-2

Print publication date: 01/12/2014

Online publication date: 27/09/2014

ISSN (print): 0006-8950

ISSN (electronic): 1460-2156

Publisher: OXFORD UNIV PRESS

URL: http://dx.doi.org/10.1093/brain/awu267

DOI: 10.1093/brain/awu267

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