alpha-Thalassemia reduces the hemolytic rate in homozygous sickle-cell disease

N Engl J Med. 1983 Jul 21;309(3):189-90. doi: 10.1056/NEJM198307213090320.
No abstract available

Publication types

  • Letter

MeSH terms

  • Adolescent
  • Anemia, Sickle Cell / blood*
  • Erythrocyte Aging
  • Female
  • Hemolysis*
  • Homozygote
  • Humans
  • Male
  • Thalassemia / blood*