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Functional Mitochondrial Heterogeneity in Heteroplasmic Cells Carrying the Mitochondrial DNA Mutation Associated with the MELAS Syndrome (Mitochondrial Encephalopathy, Lactic Acidosis, and Strokelike Episodes)

Annette C. Bakker, C. Barthélémy, Paule Frachon, Danielle Château, Damien Sternberg, Jean Pierre Mazat, Anne Lombès

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Key concepts: Heteroplasmy, Mitochondrial DNA, MELAS syndrome, Biology, Mitochondrial myopathy, Mutation, Lactic acidosis, Mitochondrion

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Functional Mitochondrial Heterogeneity in Heteroplasmic Cells Carrying the Mitochondrial DNA Mutation Associated with the MELAS Syndrome (Mitochondrial Encephalopathy, Lactic Acidosis, and Strokelike Episodes) — Research Paper | ScholarLens