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Phenotypic Spectrum Associated with Mutations of the Mitochondrial Polymerase y Gene
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Mitochondrial Neurogastrointestinal Encephalomyopathy (MMGIE) :Clin Biochem & Genetic Features of Auto Recess Mitochond Disorder
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Ekbom's Syndrome:Lypomas, Ataxia, and Neuropathy with MERRF
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Ophthalmologic Manifestations in MELAS Syndrome
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Mitochondrial DNA Deletions in Progressive External Ophthalmoplegia and Kearns-Sayre Syndrome
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Cytochrome c Oxidase Deficiency in Leigh Syndrome
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Mitochondrial Myopathies
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