Heterogeneity of beta-thalassemia in Azerbaidzhan

Haematologia (Budap). 1984;17(4):473-81.

Abstract

Globin chain synthesis, RNA and DNA of beta-thalassemic patients from Azerbaidzhan were analyzed. A beta-mRNA deficiency was found in beta +-thalassemic reticulocytes. In one case of beta +-thalassemia, it was possible to study nuclear and cytoplasmic RNA from spleen erythroid cells. The alpha/beta mRNAs sequence ratio was 5 in the nuclear and cytoplasmic RNAs. In patients with beta o-thalassemia a different level of beta-globin mRNA was demonstrated. Gene mapping analysis indicated that the general organization of the beta-globin gene was normal in the investigated cases of beta-thalassemia.

MeSH terms

  • Azerbaijan
  • Base Sequence
  • DNA / analysis
  • Globins / biosynthesis
  • Globins / genetics*
  • Humans
  • Nucleic Acid Hybridization
  • RNA, Messenger / analysis
  • Thalassemia / genetics*

Substances

  • RNA, Messenger
  • Globins
  • DNA