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Haematologica
(Sep 2019)
Children with sickle cell anemia and APOL1 genetic variants develop albuminuria early in life
Rima S. Zahr,
Evadnie Rampersaud,
Guolian Kang,
Mitchell J. Weiss,
Gang Wu,
Robert L. Davis,
Jane S. Hankins,
Jeremie H. Estepp,
Jeffrey Lebensburger
Affiliations
Rima S. Zahr
Division of Pediatric Nephrology and Hypertension, University of Tennessee Health Science Center, Memphis, TN
Evadnie Rampersaud
Department of Computational Biology, St. Jude Children’s Research Hospital, Memphis, TN
Guolian Kang
Department of Biostatistics, St. Jude Children’s Research Hospital, Memphis, TN
Mitchell J. Weiss
Department of Hematology, St. Jude Children’s Research Hospital, Memphis, TN
Gang Wu
Department of Computational Biology, St. Jude Children’s Research Hospital, Memphis, TN
Robert L. Davis
Biomedical Informatics, University of Tennessee Health Science Center, Memphis, TN
Jane S. Hankins
Department of Hematology, St. Jude Children’s Research Hospital, Memphis, TN
Jeremie H. Estepp
Department of Hematology, St. Jude Children’s Research Hospital, Memphis, TN
Jeffrey Lebensburger
Division Pediatric Hematology and Oncology, University of Alabama at Birmingham, Birmingham, AL, USA
DOI
https://doi.org/10.3324/haematol.2018.212779
Journal volume & issue
Vol. 104, no. 9
Abstract
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No abstracts available.
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