Children with sickle cell anemia and APOL1 genetic variants develop albuminuria early in life

被引：29
作者：
Zahr, Rima S. [1 ]
Rampersaud, Evadnie [2 ]
Kang, Guolian [3 ]
Weiss, Mitchell J. [4 ]
Wu, Gang [2 ]
Davis, Robert L. [5 ]
Hankins, Jane S. [4 ]
Estepp, Jeremie H. [4 ]
Lebensburger, Jeffrey [6 ]
机构：
[1] Univ Tennessee, Ctr Hlth Sci, Div Pediat Nephrol & Hypertens, Memphis, TN 38163 USA
[2] St Jude Childrens Res Hosp, Dept Computat Biol, 332 N Lauderdale St, Memphis, TN 38105 USA
[3] St Jude Childrens Res Hosp, Dept Biostat, 332 N Lauderdale St, Memphis, TN 38105 USA
[4] St Jude Childrens Res Hosp, Dept Hematol, 332 N Lauderdale St, Memphis, TN 38105 USA
[5] Univ Tennessee, Ctr Hlth Sci, Biomed Informat, Memphis, TN 38163 USA
[6] Univ Alabama Birmingham, Div Pediat Hematol & Oncol, Birmingham, AL 35294 USA
来源：
HAEMATOLOGICA | 2019年 / 104卷 / 09期
关键词：
CHRONIC KIDNEY-DISEASE; RISK VARIANTS; PROGRESSION; RACE;
D O I：
10.3324/haematol.2018.212779
中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
引用
收藏
页数：3
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