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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主要な著者: Nasrollah SALEH-GOHARI (著者), Kolsoum SAEIDI (著者), Sima ZIAADINI-DASHTKHAKI (著者)
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出版事項: Tehran University of Medical Sciences, 2020-04-01T00:00:00Z.
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3rd Floor Main Library

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