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; 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

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

Document type :

Journal articles

Domain :

Life Sciences [q-bio]

Life Sciences [q-bio] / Human health and pathology

Complete list of metadatas

https://hal-riip.archives-ouvertes.fr/pasteur-02056171
Contributor : Abdelhakim Ben Hassine <>
Submitted on : Monday, March 4, 2019 - 2:29:19 PM
Last modification on : Wednesday, May 15, 2019 - 9:27:15 AM
Long-term archiving on : Wednesday, June 5, 2019 - 3:19:57 PM

Mitochondrial Myopathy.pdf

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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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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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