Reply: Mutations in the CHCHD10 gene are a common cause of familial amyotrophic lateral sclerosis - Université Paris Cité Accéder directement au contenu
Article Dans Une Revue Brain - A Journal of Neurology Année : 2014

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

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hal-02108988 , version 1 (24-04-2019)

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Sylvie Bannwarth, Samira Ait-El-Mkadem, Annabelle Chaussenot, Emmanuelle Génin, Sandra Lacas-Gervais, et al.. Reply: Mutations in the CHCHD10 gene are a common cause of familial amyotrophic lateral sclerosis. Brain - A Journal of Neurology , 2014, 137 (12), pp.e312-e312. ⟨10.1093/brain/awu267⟩. ⟨hal-02108988⟩
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