The Spectrum of Mutations in 100 Thalassemic Carriers Referred to Ghaem Hospital of Mashhad
نویسندگان
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چکیده
Abstract Background Thalassemia is common in the Iranian population, and it must be considered in the differential diagnosis of the microcytic hypochromic anemia. The molecular analysis of β-thalassemia is necessary for prenatal molecular diagnosis. Α-thalassemia caused by loss of function of either one of the two duplicated α-globin genes or ...
