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Myotonic Dystrophy: Etiology, Clinical Features, and Diagnosis
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Making Sense of the Clinical Spectrum of Limb Girdle Muscular Dystrophies
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Progressive Development of Cardiomyopathy Following Altered Autonomic Activity in Status Epilepticus
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MELAS
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Mitochondrial DNA Polymerase-y and Human Disease
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Clinical and Genetic Abnormalities in Patients with Friedreich's Ataxia
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Mitochondrial DNA and Disease
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Stroke in Pediatric Acquired Immunodeficiency Syndrome
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Mendelian Etiologies of Stroke
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