Τρίτη 17 Νοεμβρίου 2020

Argyrophilic Nucleolar Organizing Regions in Patients with Xeroderma Pigmentosum Group E

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Abstract

Xeroderma pigmentosum E (XP‐E) is a rare autosomal recessive inherited genodermatosis associated with less severe sun burning with minimal sun exposure. The affected individuals acquire abnormal pigmentation and are at high risk for skin cancer [1]. Notably, the DNA damage‐binding protein 2 (DDB2) gene is responsible for XP‐ E disease [2].

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