Relationship between erythropoietin and hepcidin among transfused Malaysian adult thalassemic patients

Thalassemia is a genetic blood disorder characterized by insufficient hemoglobin level or due to mutation in the globin chains causing an anemic condition with iron overload despite no history of transfusion; thus, insufficient hemoglobin will cause an imbalance of erythropoietin (an endogenously pr...

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Bibliographic Details
Main Author: Ibraheem, Shahad Mohammed
Format: Thesis
Published: 2022
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