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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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