Genetic association of a gain of function interferon gamma receptor 1 (IFNGR1) polymorphism and the intergenic region LNCAROD/DKK1 with Behçet's disease.

Ortiz Fernández, Lourdes; Coit, Patrick; Yilmaz, Vuslat; Yentür, Sibel; Alibaz-Oner, FATMA; Aksu, Kenan; Erken, Eren; Düzgün, Nursen; Keser, Gokhan; Cefle, Ayse; Yazici, Ayten; Ergen, Andac; Alpsoy, Erkan; Salvarani, Carlo; Casali, Bruno; Kısacık, Bünyamin; Kötter, Ina; Henes, Jörg; Çınar, Muhammet; Schaefer, Arne; Nohutcu, Rahime; Zhernakova, Alexandra; Wijmenga, Cisca; Takeuchi, Fujio; Harihara, Shinji; Kaburaki, Toshikatsu; Messedi, Meriam; Song, Yeong-Wook; Kaşifoğlu, Timuçin; Carmona, F; Guthridge, Joel; James, Judith; Martin, Javier; González Escribano, María; Saruhan-Direskeneli, Güher; Direskeneli, RAFİ; Sawalha, Amr

doi:10.1002/art.41637

Genetic association of a gain of function interferon gamma receptor 1 (IFNGR1) polymorphism and the intergenic region LNCAROD/DKK1 with Behçet's disease.

Ortiz Fernández L., Coit P., Yilmaz V., Yentür S. P., Alibaz-Oner F., Aksu K., ...Daha Fazla

Arthritis & rheumatology (Hoboken, N.J.), cilt.73, ss.1244-1252, 2021 (SCI-Expanded)

Yayın Türü: Makale / Tam Makale
Cilt numarası: 73
Basım Tarihi: 2021
Doi Numarası: 10.1002/art.41637
Dergi Adı: Arthritis & rheumatology (Hoboken, N.J.)
Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED)
Sayfa Sayıları: ss.1244-1252
Marmara Üniversitesi Adresli: Evet

Özet

Objective Behcet's disease is a complex systemic inflammatory vasculitis of incompletely understood etiology. This study was undertaken to investigate genetic associations with Behcet's disease in a diverse multiethnic population.