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Reply: A distinct clinical phenotype in a German kindred with motor neuron disease carrying a CHCHD10 mutation

Lookup NU author(s): 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: 2015

Volume: 138

Online publication date: 12/02/2015

Acceptance date: 01/01/1900

ISSN (print): 0006-8950

ISSN (electronic): 1460-2156

Publisher: OXFORD UNIV PRESS

URL: http://dx.doi.org/10.1093/brain/awv015

DOI: 10.1093/brain/awv015


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