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

Author： Sohl Christal D.   Kasiviswanathan Rajesh   Copeland William C.   Anderson Karen S.  

Publisher： Oxford University Press

ISSN： 1460-2083

Source： Human Molecular Genetics, Vol.22, Iss.6, 2013-03, pp. : 1074-1085

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