4.0 Article

Broader Spectrum of β-Thalassemia Mutations in Oman: Regional Distribution and Comparison with Neighboring Countries

Journal

HEMOGLOBIN
Volume 39, Issue 2, Pages 107-110

Publisher

TAYLOR & FRANCIS LTD
DOI: 10.3109/03630269.2015.1009632

Keywords

beta Gene mutation spectrum; beta-thalassemia (beta-thal); Oman

Ask authors/readers for more resources

The objective of this study was to expand and study the molecular spectrum of beta-thalassemia (beta-thal) mutations in Oman by examining cases from seven different regions and comparing the prevalence with neighboring countries. A total of 446 cases of beta hemoglobinopathies was obtained and analyzed to determine the frequency and distribution of the different beta alleles. The molecular spectrum of beta-thal in Oman revealed the presence of 32 mutations from different origins and 11 alleles are reported for the first time in the Omani population. The wide heterogeneous spectrum of beta-thal mutations found can be associated with the history of trade and migration as well as the past domination from other countries. The presented data will facilitate the development of a comprehensive prevention strategy in Oman.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.0
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available