Journal:
:iranian journal of immunology
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morteza bagheri
department of molecular biology & genetics, uromia university of medical sciences, uromia, iran ali akbar amirzargar
immunogenetic laboratory, department of immunology, school of medicine, tehran university of
medical sciences ardeshir ghavamzadeh
hematology-oncology and bmt research center, shariati hospital, tehran, iran kamran alimoghadam
hematology-oncology and bmt research center, shariati hospital, tehran, iran farideh khosravi
immunogenetic laboratory, department of immunology, school of medicine, tehran university of
medical sciences bita ansaripour
immunogenetic laboratory, department of immunology, school of medicine, tehran university of
medical sciences batoul moradi
background: β-thalassemia as a hereditary disease is defined as defective synthesis of β-globin chains, resulting in erythropoiesis abnormalities and severe anemia. different studies have shown that cytokines and cytokine gene polymorphisms play a major role in the pathogenesis of β-thalassemia. single nucleotide polymorphisms (snps) within the promoter region or other regulatory sequences ...
