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Structural and function impact of ERCC2 gene variants in Xeroderma pigmentosum: An integrative computational and docking analysis

Xeroderma pigmentosum (XP) is a rare inherited disorder that causes extreme sensitivity to sunlight, leading to early-onset skin lesions, eye complications, and a higher risk of developing tumors. The disease occurs due to defects in the DNA repair system, especially in the ERCC2 gene, which encodes...

Ausführliche Beschreibung

Gespeichert in:
Hauptverfasser: Aman Ullah, Memona Aslam, Seema Ismael, Maqsood Ahmad, Ali Umar, Misbah Ullah Khan, Muhammad Saleem Khan
Format: Artigo
Sprache:Inglês
Veröffentlicht: Elsevier 2025-01-01
Schriftenreihe:In Silico Research in Biomedicine
Schlagworte:
ERCC2
XP
Docking
Mutations
MD simulation
FT
Online-Zugang:http://www.sciencedirect.com/science/article/pii/S3050787125001106
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