Haplotype Analysis in Carriers of β-Globin Gene Mutation Facil-itates Genetic Counseling in β-Thalassemia: A Cross-Sectional Study in Kerman Province, Iran
Background: β-thalassemia is characterized by reduced synthesis of the hemoglobin beta chain that results in microcytic hypochromic anemia and reduced amounts of hemoglobin A (HbA) on hemoglobin analysis. β-thalassemias are caused by mutations in the β-globin gene, inherited in an autosomal recessiv...
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Tehran University of Medical Sciences,
2020-04-01T00:00:00Z.
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