“In Vitro” Scf Treatment Downregulates Fpn1 And Gdf15 Mrna Expression In Human Beta-Thalassemic Eryt

来源 :The 35th World Congress of the International Society of Hema | 被引量 : 0次 | 上传用户:liuqingsong835200
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Background And Aims Progressive iron overload is the most important and fatal complication in beta-thalassemia.However,little is known about the relationship among ineffective erythropoiesis,the role of iron-regulatory genes,and tissue iron distribution in β-thalassemia.
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