Familial Melanoma Phenotype With Xeroderma Pigmentosum Group C (XP-C) Genotype - The Putative Role of MC1R Polymorphism as Modifier

• Main Authors: Franciele Antonieta Bianchi Leidenz (Author), Flavia Vasques Bittencourt (Author), Williana Garcia Braga (Author), Ellio Magno de Sá Araujo (Author), Carolina Cavalieri Gomes (Author), Vanessa de Fatima Bernardes (Author), Eitan Friedman (Author), Luiz De Marco (Author)
• Format: Knjiga
• Izdano: Mattioli1885, 2024-01-01T00:00:00Z.
• Teme: article
• Online dostop: Connect to this object online.

Introduction: Xeroderma pigmentosum (XP), a rare inherited condition, hallmarked by extreme sensitivity to sun exposure resulting in multiple skin cancers and non-malignant skin alterations is attributed to homozygous inactivating pathogenic variants (PVs) in DNA repair genes, predominantly the XPC...