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Oxford University Press

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Introducing the human Leigh syndrome mutation T9176G into Saccharomyces cerevisiae mitochondrial DNA leads to severe defects in the incorporation of Atp6p into the ATP synthase and in the mitochondrial morphology

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Regulation and Modulation of Human DNA Polymerase δ Activity and Function

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Genes, Vol. 8, Iss. 7, 2017-07 ,pp. : 190-190

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Mutation and selection at silent and replacement sites in the evolution of animal mitochondrial DNA

By Rand D.M.   Kann L.M.  

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Mutation dependance of the mitochondrial DNA copy number in the first stages of human embryogenesis

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