Frontiers | Case Report: Identification of Novel Variants in ERCC4 and DDB2 Genes in Two Tunisian Patients With Atypical Xeroderma Pigmentosum Phenotype
Abbreviations FH: Familial hypercholesterolemia; MDM: Mal de Meleda;... | Download Scientific Diagram
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Genes | Free Full-Text | Clinical and Mutational Spectrum of Xeroderma Pigmentosum in Egypt: Identification of Six Novel Mutations and Implications for Ancestral Origins
Cancers | Free Full-Text | The French Cohort of DNA Repair-Deficient Xeroderma Pigmentosum Patients: Risk of Hematological Malignancies
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Xeroderma pigmentosum: report of two cases and review of ... - JPAD
Cells | Free Full-Text | Reappraisal of the Concept of Accelerated Aging in Neurodegeneration and Beyond
Cancers | Free Full-Text | The French Cohort of DNA Repair-Deficient Xeroderma Pigmentosum Patients: Risk of Hematological Malignancies
Frontiers | Xeroderma Pigmentosum C (XPC) Mutations in Primary Fibroblasts Impair Base Excision Repair Pathway and Increase Oxidative DNA Damage
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Cancers | Free Full-Text | The French Cohort of DNA Repair-Deficient Xeroderma Pigmentosum Patients: Risk of Hematological Malignancies
Xeroderma Pigmentosum Pakistan
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An Xpd mouse model for the combined xeroderma pigmentosum/Cockayne syndrome exhibiting both cancer predisposition and segmental progeria.