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Haematologica. 2017 Jan;102(1):e1-e6. doi: 10.3324/haematol.2016.154153. Epub 2016 Sep 22.

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

Author information

1
Division of Hematology & Oncology, Department of Medicine, Comprehensive Sickle Cell Center, University of Illinois at Chicago, IL, USA ssaraf@uic.edu.
2
Division of Hematology & Oncology, Department of Medicine, Comprehensive Sickle Cell Center, University of Illinois at Chicago, IL, USA.
3
Department of Pharmacy Practice, College of Pharmacy, University of Illinois at Chicago, IL, USA.
4
Department of Public Health Sciences, Loyola University Chicago Stritch School of Medicine, Maywood, IL, USA.
5
Division of Pulmonary and Critical Care Medicine, Department of Medicine, University of Illinois at Chicago, IL, USA.
6
Division of Nephrology, Department of Medicine, University of Illinois at Chicago, IL, USA.
PMID:
27658436
PMCID:
PMC5210238
DOI:
10.3324/haematol.2016.154153
[Indexed for MEDLINE]
Free PMC Article

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