Black β-thalassemia homozygotes with specific sequence variations in the 5′ hypersensitive site-2 of the locus control region have high levels of fetal hemoglobin.

Autor: Beris, Ph., Kitundu, M. N., Baysal, E., Öner, C., Lanclos, K. D., Dimovski, A. J., Kutlar, F., Huisman, T. H. J.
Zdroj: American Journal of Hematology; 1992, Vol. 41 Issue 2, p97-101, 5p
Databáze: Complementary Index