Reply: A distinct clinical phenotype in a German kindred with motor neuron disease carrying a CHCHD10 mutation.
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| Description | scientific article published on 12 February 2015 |
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author: Valérie Serre Emmanuelle C Genin Francoise Lespinasse Patrick Yu-Wai-Man |
| Publication date | February 12, 2015 |
| Language | English |
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| Missing/wrong data? | Edit Wikidata item |