Haplotype Analysis in Carriers of β-Globin Gene Mutation Facil-itates Genetic Counseling in β-Thalassemia: A Cross-Sectional Study in Kerman Province, Iran

• 主要な著者: Nasrollah SALEH-GOHARI (著者), Kolsoum SAEIDI (著者), Sima ZIAADINI-DASHTKHAKI (著者)
• フォーマット: 図書
• 出版事項: Tehran University of Medical Sciences, 2020-04-01T00:00:00Z.
• 主題: article
• オンライン･アクセス: Connect to this object online.

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...