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Russian Journal of Genetics, Vol. 42, Iss. 1, 2006-01 ,pp. : 84-88

MAIK Nauka/Interperiodica

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Modulation of the W748S mutation in DNA polymerase  by the E1143G polymorphismin mitochondrial disorders

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Functional defects due to spacer-region mutations of human mitochondrial DNA polymerase in a family with an ataxia-myopathy syndrome

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Mutations in human DNA polymerase γ confer unique mechanisms of catalytic deficiency that mirror the disease severity in mitochondrial disorder patients

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Polymorphism in the activity of human crossover hotspots independent of local DNA sequence variation

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