Epidemiology of A3243G, the Mutation for Mitochondrial Encephalomyopathy, Lactic Acidosis, and Strokelike Episodes: Prevalence of the Mutation in an Adult Population

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Encephalopathy, Lactic Acidosis, and Strokelike Episodes

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Human mitochondrial leucyl-tRNA synthetase corrects mitochondrial dysfunctions due to the tRNALeu(UUR) A3243G mutation, associated with mitochondrial encephalomyopathy, lactic acidosis, and stroke-like symptoms and diabetes.

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ژورنال

عنوان ژورنال: The American Journal of Human Genetics

سال: 1998

ISSN: 0002-9297

DOI: 10.1086/301959