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The mitochondrial tRNA(Leu(UUR)) mutation in mitochondrial encephalomyopathy, lactic acidosis, and strokelike episodes (MELAS): genetic, biochemical, and morphological correlations in skeletal muscle

The study involved 219 participants with T1DM from the Joslin kidney study, 144 with T2DM also from the Joslin cohort, and 162 individuals with diabetes from the Pima Indian study

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