Analysis of the genetic component of systemic sclerosis in Iranian and Turkish populations through a genome-wide association study
RHEUMATOLOGY, cilt.58, sa.2, ss.289-298, 2019 (SCI-Expanded, Scopus)
- Yayın Türü: Makale / Tam Makale
- Cilt numarası: 58 Sayı: 2
- Basım Tarihi: 2019
- Doi Numarası: 10.1093/rheumatology/key281
- Dergi Adı: RHEUMATOLOGY
- Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
- Sayfa Sayıları: ss.289-298
- Anahtar Kelimeler: SSc, GWAS, Iranian and Turkish populations, risk loci, FUNCTIONAL POLYMORPHISM, SUSCEPTIBILITY LOCI, KAPPA-B, IDENTIFICATION, REVEALS, DISEASE, REGION, RISK, MHC
- Marmara Üniversitesi Adresli: Evet
Özet
Objectives. SSc is an autoimmune disease characterized by alteration of the immune response, vasculopathy and fibrosis. Most genetic studies on SSc have been performed in European-ancestry populations. The aim of this study was to analyse the genetic component of SSc in Middle Eastern patients from Iran and Turkey through a genome-wide association study.