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: muscle biopsy; genetics; respiratory chain; mitochondrial; mtDNA

Domains: Life Sciences [q-bio]; Human health and pathology

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⟩