Determination of alpha hemoglobin stabilizing protein (AHSP) gene expression and oxidative stress parameters in HbE/beta-Thalassemia

Beta-Thalassaemia is the genetic disorders of haemoglobin synthesis characterized by reduced or absent β-globin chain synthesis thus lead to imbalance of tetramer. The Alpha Haemoglobin Stabilizing Protein (AHSP) acts as a molecular chaperone for α-globin by stabilizing free α-globin preventing it f...

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Bibliographic Details
Main Author:	Yaacob, Nur Suraya Che
Format:	Thesis
Language:	English
Published:	2021
Subjects:	RK Dentistry
Online Access:	http://eprints.usm.my/50464/
Abstract	Abstract here

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