APOL1 , α-thalassemia, and BCL11A variants as a genetic risk profile for progression of chronic kidney disease in sickle cell anemia - Saraf, Santosh L.; Shah, Binal N.; Zhang, Xu; Han, Jin; Tayo, Bamidele O.; Abbasi, Taimur; Ostrower, Adam; Guzman, Elizabeth; Molokie, Robert E.; Gowhari, Michel; Hassan, Johara; Jain, Shivi; et al. (Haematologica (Roma), 2017)
Keywords: Adult; alpha-Thalassemia - complications; alpha-Thalassemia - genetics; Anemia, Sickle Cell; Apolipoprotein L1 - genetics; Carrier Proteins - genetics; Female; Humans; Male; Nuclear Proteins - genetics; Online Only; Renal Insufficiency, Chronic - etiology; Renal Insufficiency, Chronic - genetics; Risk Factors