Beta-Globin Gene Cluster Haplotypes in Iranian Sickle Cell Patients: Relation to Some Hematologic

نویسندگان
Jaseb, k ID 1
Zandian, KH ID 2
Samadi, B ID 3
Keikhaei, B ID 4
Galehdari, H ID 5
Pedram, M ID 6
Bashirpour, SH ID 7

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چکیده

Background: Sickle cell anemia is relatively common in Khuzestan province located in Southwest Iran. The characteristics of sickle cell disease in Iran are apparently different from other regions some of these characteristics might be related to β-chain haplotypes. The purpose of this study was to determine the frequency of β-chain ...

کلیدواژه‌ها
Sickle cell anemia, haplotypes, hemoglobin, fetal, Iran