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

de Ceulaer, K

alpha-Thalassemia reduces the hemolytic rate in homozygous sickle-cell disease. [electronic resource] - The New England journal of medicine Jul 1983 - 189-90 p. digital

Publication Type: Letter

0028-4793

10.1056/NEJM198307213090320 doi


Adolescent
Anemia, Sickle Cell--blood
Erythrocyte Aging
Female
Hemolysis
Homozygote
Humans
Male
Thalassemia--blood