Mutations in human DNA polymerase γ confer unique mechanisms of catalytic deficiency that mirror the disease severity in mitochondrial disorder patients (Q36626862)

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scientific article published on 3 December 2012
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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
scientific article published on 3 December 2012

    Statements

    Mutations in human DNA polymerase γ confer unique mechanisms of catalytic deficiency that mirror the disease severity in mitochondrial disorder patients (English)
    Christal D Sohl
    Rajesh Kasiviswanathan
    William C Copeland
    Karen S Anderson
    3 December 2012
    1074-1085

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