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Reply: A distinct clinical phenotype in a German kindred with motor neuron disease carrying a CHCHD10 mutation.
scientific article published on 12 February 2015
Author/s
author: Emmanuelle C Genin, Valérie Serre, Francoise Lespinasse, Patrick Yu-Wai-Man
Work details
Publication date
February 12, 2015
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Language
English
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