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MELAS Syndrome Involving a Mother & Two Children
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A Young Man with Progressive Vision and Hearing Loss
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Mitochondrial Encephalomyopathy, Lactic Acidosis, Stroke-Like Episodes (MELAS) :Clinical, Radiological, Pathol & Genetic Observ
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The Polymerase Chain Reaction:Application to Nervous System Disease
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The Neuropsychological Features of Mitochondrial Myopathies and Encephalomyopathies
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A Mitochondrial DNA Mutation as a Cause of Leber's Hereditary Optic Neuropathy
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