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

Haematologica. 2019 Sep;104(9):e385-e387. doi: 10.3324/haematol.2018.212779. Epub 2019 Mar 19.
No abstract available

Publication types

  • Letter

MeSH terms

  • Adolescent
  • Albuminuria / complications*
  • Albuminuria / genetics*
  • Alleles
  • Anemia, Sickle Cell / complications*
  • Anemia, Sickle Cell / genetics*
  • Apolipoprotein L1 / genetics*
  • Case-Control Studies
  • Child
  • Female
  • Genetic Variation
  • Genotype
  • Homozygote
  • Humans
  • Kaplan-Meier Estimate
  • Male
  • Mutation
  • Risk
  • beta-Globins / genetics*

Substances

  • APOL1 protein, human
  • Apolipoprotein L1
  • beta-Globins