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Explosive mutation accumulation triggered by heterozygous human Pol ε proofreading-deficiency is driven by suppression of mismatch repair.

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第一作者: Karl P,Hodel
第一单位: Department of Biochemistry and Molecular Biology, Tulane University School of Medicine, New Orleans, United States.
作者单位: Department of Biochemistry and Molecular Biology, Tulane University School of Medicine, New Orleans, United States. [1] Program in Genetics and Genome Biology, The Hospital for Sick Children, Toronto, Canada. [2] The Arthur and Sonia Labatt Brain Tumour Research Centre, The Hospital for Sick Children, Toronto, Canada.;Institute of Medical Science, Faculty of Medicine, University of Toronto, Toronto, Canada. [3] Department of Pathology, Tulane University School of Medicine, New Orleans, United States. [4] Department of Pharmacology, Tulane University School of Medicine, New Orleans, United States.;Tulane Center for Stem Cell Research and Regenerative Medicine, Tulane University School of Medicine, New Orleans, United States. [5] Program in Genetics and Genome Biology, The Hospital for Sick Children, Toronto, Canada.;The Arthur and Sonia Labatt Brain Tumour Research Centre, The Hospital for Sick Children, Toronto, Canada.;Division of Hematology/Oncology, The Hospital for Sick Children, Toronto, Canada. [6] Program in Genetics and Genome Biology, The Hospital for Sick Children, Toronto, Canada.;Department of Paediatric Laboratory Medicine, The Hospital for Sick Children, Toronto, Canada.;Department of Laboratory Medicine and Pathobiology, University of Toronto, Toronto, Canada. [7] Department of Biochemistry and Molecular Biology, Tulane University School of Medicine, New Orleans, United States.;Tulane Cancer Center, Tulane University School of Medicine, New Orleans, United States. [8]
DOI 10.7554/eLife.32692
PMID 29488881
发布时间 2022-04-06
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