Decrease of 3243 A–>G mtDNA mutation from blood in MELAS syndrome: a longitudinal study

Rahman, S., Poulton, J., Marchington, D., Suomalainen, A.·2001·The American Journal of Human Genetics

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  24. Response to Letter regarding case report, “Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes due to m.3243A > G mutation in a 76-year-old woman”
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