Relationship between erythropoietin and hepcidin among transfused Malaysian adult thalassemic patients

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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
Language:	English
Published:	2022
Subjects:	Thalassemia Erythropoietin Hepcidins
Online Access:	http://psasir.upm.edu.my/id/eprint/103847/ http://psasir.upm.edu.my/id/eprint/103847/1/Shahad%20Mohammed%20Ibraheem%20-%20IR.pdf

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