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High mutational burden in colorectal carcinomas with monoallelic POLE mutations: absence of allelic loss and gene promoter methylation.,Modern Pathology - X-MOL
Exome sequencing reveals a de novo POLD1 mutation causing phenotypic variability in mandibular hypoplasia, deafness, progeroid f
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POLD1: Central mediator of DNA replication and repair, and implication in cancer and other pathologies | Semantic Scholar
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POLE/POLD1 mutation and tumor immunotherapy | Journal of Experimental & Clinical Cancer Research | Full Text
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Combined immunodeficiency caused by a loss-of-function mutation in DNA polymerase delta 1 - ScienceDirect
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Mutation spectrum of POLE and POLD1 mutations in South East Asian women presenting with grade 3 endometrioid endometrial carcinomas - ScienceDirect
Exome sequencing reveals a de novo POLD1 mutation causing phenotypic variability in mandibular hypoplasia, deafness, progeroid f
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POLD1 Germline Mutations in Patients Initially Diagnosed with Werner Syndrome - Lessel - 2015 - Human Mutation - Wiley Online Library
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DNA Polymerase Delta 1 Catalytic Subunit (POLD1) as a Prognostic Factor in Clear Cell Renal Cell Carcinoma Patients | In Vivo
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Top mutated DNA polymerases and mutation prevalence in Fanconi anemia... | Download Scientific Diagram
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POLD1: Central mediator of DNA replication and repair, and implication in cancer and other pathologies - ScienceDirect
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