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Dive into the research topics of 'Reply: Mutations in the CHCHD10 gene are a common cause of familial amyotrophic lateral sclerosis'. Together they form a unique fingerprint.- Sort by
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Sylvie Bannwarth, Samira Ait-El-Mkadem, Annabelle Chaussenot, Emmanuelle C. Genin, Sandra Lacas-Gervais, Konstantina Fragaki, Laetitia Berg-Alonso, Yusuke Kageyama, Valérie Serre, David Moore, Annie Verschueren, Cécile Rouzier, Isabelle Le Ber, Gaëlle Augé, Charlotte Cochaud, Françoise Lespinasse, Karine N'Guyen, Anne De Septenville, Alexis Brice, Patrick Yu-Wai-Man
Research output: Contribution to journal › Letter › peer-review