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American Journal Of Medical Genetics Part A, Vol. 167, Iss. 12, 2015-12 ,pp. : 2975-2984

John Wiley & Sons Inc

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A novel frameshift mutation of the mtDNA COIII gene leads to impaired assembly of cytochrome c oxidase in a patient affected by Leigh-like syndrome

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Oxford University Press

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Metabolic consequences of a novel missense mutation of the mtDNA CO I gene

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Oxford University Press

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Updating the East Asian mtDNA phylogeny: a prerequisite for the identification of pathogenic mutations

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The role of mtDNA background in disease expression: a new primary LHON mutation associated with Western Eurasian haplogroup J

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Springer Publishing Company

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