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