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

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

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Bannwarth, Sylvie | Ait-El-Mkadem, Samira | Chaussenot, Annabelle | Genin, Emmanuelle C | Lacas-Gervais, Sandra | Fragaki, Konstantina | Berg-Alonso, Laetitia | Kageyama, Yusuke | Serre, Valérie | Moore, David | Verschueren, Annie | Rouzier, Cécile | Le Ber, Isabelle | Augé, Gaëlle | Cochaud, Charlotte | Lespinasse, Françoise | N'Guyen, Karine | de Septenville, Anne | Brice, Alexis | Yu-Wai-Man, Patrick | Sesaki, Hiromi | Pouget, Jean | Paquis-Flucklinger, Véronique

Edité par CCSD ; Oxford University Press -

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Langue: en

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