Reply: A distinct clinical phenotype in a German kindred with motor neuron disease carrying a CHCHD10 mutation. - Université Paris Cité Accéder directement au contenu
Article Dans Une Revue Brain - A Journal of Neurology Année : 2015

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

Jean Pouget
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Neurobiologie

Dates et versions

hal-01218555 , version 1 (21-10-2015)

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Sylvie Bannwarth, Samira Ait-El-Mkadem, Annabelle Chaussenot, Emmanuelle C Genin, Sandra Lacas-Gervais, et al.. Reply: A distinct clinical phenotype in a German kindred with motor neuron disease carrying a CHCHD10 mutation.. Brain - A Journal of Neurology , 2015, 138 (Pt 9), pp.e377. ⟨hal-01218555⟩
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