Genetic Association of a Gain‐of‐Function IFNGR1 Polymorphism and the Intergenic Region LNCAROD/DKK1 With Behçet’s Disease

Objective Behçet’s disease is a complex systemic inflammatory vasculitis of incompletely understood etiology. This study was undertaken to investigate genetic associations with Behçet’s disease in a diverse multiethnic population. Methods A total of 9,444 patients and controls from 7 different popul...

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Veröffentlicht in:Arthritis & rheumatology (Hoboken, N.J.) N.J.), 2021-07, Vol.73 (7), p.1244-1252
Hauptverfasser: Ortiz Fernández, Lourdes, Coit, Patrick, Yilmaz, Vuslat, Yentür, Sibel P., 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 M., Zhernakova, Alexandra, Wijmenga, Cisca, Takeuchi, Fujio, Harihara, Shinji, Kaburaki, Toshikatsu, Messedi, Meriam, Song, Yeong‐Wook, Kaşifoğlu, Timuçin, Carmona, F. David, Guthridge, Joel M., James, Judith A., Martin, Javier, González Escribano, María Francisca, Saruhan‐Direskeneli, Güher, Direskeneli, Haner, Sawalha, Amr H.
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Sprache:eng
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