Arg399Gln Polymorphism of the XRCC1 Gene is Associated with Coronary Artery Disease in a Turkish Population

Ozbilum, N.; Arslan, SERDAL; Yanartas, M.; Yilmaz, Z.; Berkan, O.

doi:10.7727/wimj.2015.057

Arg399Gln Polymorphism of the XRCC1 Gene is Associated with Coronary Artery Disease in a Turkish Population

Ozbilum N., Arslan S., Yanartas M., Yilmaz Z., Berkan O.

WEST INDIAN MEDICAL JOURNAL, cilt.66, sa.6, 2017 (SCI-Expanded)

Yayın Türü: Makale / Tam Makale
Cilt numarası: 66 Sayı: 6
Basım Tarihi: 2017
Doi Numarası: 10.7727/wimj.2015.057
Dergi Adı: WEST INDIAN MEDICAL JOURNAL
Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
Açık Arşiv Koleksiyonu: AVESİS Açık Erişim Koleksiyonu
Sivas Cumhuriyet Üniversitesi Adresli: Evet

Özet

Objective: Coronary artery disease, the leading cause of morbidity and mortality worldwide, is an inflammatory disease. The X-ray repair cross complementing 1 (XRCC1) gene plays the role of scaffolding protein for the base excision repair (BER) and single strand break (SSB) repair.