MELAS
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Mitochondrial DNA and Disease
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Metabolic Disease and Stroke: MELAS
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Mitochondrial DNA Polymerase-y and Human Disease
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Mitochondrial Respiratory-Chain Diseases
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Acute Leukoencephalopathies:Differential Diagnosis and Investigation
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Cerebral Infarction Associated with Kearns-Sayre Syndrome-Related Cardiomyopathy
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Inclusion Body Myositis and Myopathies
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Myasthenic Symptoms in Patients with Mitochondrial Myopathies
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The Polymerase Chain Reaction:Application to Nervous System Disease
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A Mitochondrial DNA Mutation as a Cause of Leber's Hereditary Optic Neuropathy
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Cytochrome c Oxidase Deficiency in Leigh Syndrome
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