Molecular nature of mutations causing beta zero-thalassaemia in Azerbaijan.

G. Y. Solovyev, A. A. Gol'tsov, V. L. Surin, E. N. Lebedenko, O. K. Kaboev, A. V. Lukianenko, A. A. Alekseev, O. V. Plutalov, T. S. Dadasheva, R. S. Rustamov

Research output: Contribution to journalArticlepeer-review

6 Citations (Scopus)


Beta zero-thalassaemia comprises a series of closely related haemoglobinopathies which are widely spread in some areas (the Mediterranean, Caucasus, Central Asia, and others). It is caused by a variety of mutations in the beta-globin gene which damage its expression, thus leading to severe illness, which is often lethal at an early age. By means of the polymerase chain reaction (PCR), restriction analysis, and sequencing by the Maxam-Gilbert method, we have identified a number of mutations in the beta-globin gene that cause beta zero-thalassaemia in the Azerbaijanian population, viz AA deletion in codon 8, C----T transition in codon 39, and a previously unknown G deletion in codons 82/83.

Original languageEnglish
Pages (from-to)300-304
Number of pages5
JournalBiomedical science
Issue number3
Publication statusPublished - Mar 1990
Externally publishedYes

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