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A specific point mutation in the mitochondrial genome of Caucasians with MELAS

C. Enter, J. M�ller-H�cker, S. Zierz, G. Kurlemann, D. Pongratz, C. F�rster, B. Obermaier–Kusser, Klaus-Dieter Gerbitz

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Key concepts: Heteroplasmy, MELAS syndrome, Mitochondrial DNA, Mitochondrial myopathy, Biology, Lactic acidosis, Mitochondrial encephalomyopathy, Point mutation

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A specific point mutation in the mitochondrial genome of Caucasians with MELAS — Research Paper | ScholarLens