Polg2 is essential for mammalian embryogenesis and is required for mtDNA maintenance

By Humble Margaret M.   Young Matthew J.   Foley Julie F.   Pandiri Arun R.   Travlos Greg S.   Copeland William C.  

Human Molecular Genetics, Vol. 22, Iss. 5, 2013-03 ,pp. : 1017-1025

Oxford University Press

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

By Monnot Sophie   Samuels David C.   Hesters Laetitia   Frydman Nelly   Gigarel Nadine   Burlet Philippe   Kerbrat Violaine   Lamazou Frédéric   Frydman René   Benachi Alexandra   Feingold Josué   Rotig Agnes   Munnich Arnold   Bonnefont Jean-Paul   Steffann Julie  

Human Molecular Genetics, Vol. 22, Iss. 9, 2013-05 ,pp. : 1867-1872

Oxford University Press

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A cluster of pathogenic mutations in the 35 exonuclease domain of DNA polymerase gamma defines a novel module coupling DNA synthesis and degradation

By Szczepanowska Karolina   Foury Franoise  

Human Molecular Genetics, Vol. 19, Iss. 18, 2010-09 ,pp. : 3516-3529

Oxford University Press

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Mitochondrial and nuclear DNA defects in Saccharomyces cerevisiae with mutations in DNA polymerase  associated with progressive external ophthalmoplegia

By Stuart Gregory R.   Santos Janine H.   Strand Micheline K.   Van Houten Bennett   Copeland William C.  

Human Molecular Genetics, Vol. 15, Iss. 2, 2006-01 ,pp. : 363-374

Oxford University Press

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

By Luoma Petri T.  

Human Molecular Genetics, Vol. 14, Iss. 14, 2005-07 ,pp. : 1907-1920

Oxford University Press

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