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

Josef Finsterer 1 Sinda Zarrouk-Mahjoub 2
1 Krankenanstalt Rudolfstiftung
2 LR11IPT05 - Laboratoire de Génomique Biomédicale et Oncogénétique - Biomedical Genomics and Oncogenetics Laboratory
Keywords : respiratory chain genetics mtDNA mitochondrial muscle biopsy
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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, Japanese Society of Internal Medicine, 2017, 56 (19), pp.2693-2693. ⟨10.2169/internalmedicine.8820-17⟩. ⟨pasteur-02056171⟩

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