Expanding phenotype of mitochondrial depletion syndrome in association with TWNK mutations
| Autor: | Sukhudyan, Biayna, Gevorgyan, Ani, Sarkissian, Ashot, Boltshauser, Eugen |
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| Zdroj: | In European Journal of Paediatric Neurology May 2019 23(3):537-540 |
| Databáze: | ScienceDirect |
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