Abstract:Thalassemia is one of the most common inherited blood disorder characterized by decrease or absent synthesis of globin chains, there are two types of thalassemia, alpha and betathalassemia (1) . Beta-thalassemia results from a defect in production of beta globin chain due to mutations in the HBB gene on chromosome 11, inherited in an autosomal recessive fashion. Beta-thalassemia major is serious blood disorder since affected individual are unable to made healthy red blood cell and dependent on blood transfusio… Show more
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