APOL1, α-thalassemia, and BCL11A variants as a genetic risk profile for progression of chronic kidney disease in sickle cell anemia

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Bibliographic Details
Published in:	Haematologica (Roma) Vol. 102; no. 1; pp. e1 - e6
Main Authors:	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, Cooper, Richard S, Machado, Roberto F, Lash, James P, Gordeuk, Victor R
Format:	Journal Article
Language:	English
Published:	Italy Ferrata Storti Foundation 01-01-2017
Subjects:	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
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Bibliography:	SourceType-Other Sources-1 ObjectType-Article-2 content type line 63 ObjectType-Correspondence-1
ISSN:	0390-6078 1592-8721
DOI:	10.3324/haematol.2016.154153