Clinicopathologic Conference, MELAS (mitochondrial encephalopathy, lactic acidosis, and stroke like episodes)
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Mitochondrial DNA Polymerase-y and Human Disease
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A 38-Year-Old Man with Respiratory Failure and Progressive Leg Weakness
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MELAS
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Mitochondrial Respiratory-Chain Diseases
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Inborn Errors of Metabolism as a Cause of Neurological Disease in Adults: An Approach to Investigation
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Exercise Intolerance Due to Mutations in the Cytochrome b Gene of Mitochondrial DNA
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Phosphorylase Deficiency
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