Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-like Episodes (MELAS) due to a m.10158T>C ND3 Mutation with a Normal Muscle Biopsy - Archive ouverte HAL Access content directly
Journal Articles Internal Medicine Year : 2017

Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-like Episodes (MELAS) due to a m.10158T>C ND3 Mutation with a Normal Muscle Biopsy

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pasteur-02056171 , version 1 (04-03-2019)

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Attribution - NonCommercial - NoDerivatives - CC BY 4.0

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Josef Finsterer, Sinda Zarrouk-Mahjoub. Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-like Episodes (MELAS) due to a m.10158T>C ND3 Mutation with a Normal Muscle Biopsy. Internal Medicine, 2017, 56 (19), pp.2693-2693. ⟨10.2169/internalmedicine.8820-17⟩. ⟨pasteur-02056171⟩

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