Association of Alpha Haemoglobin Stabilizing Protein in HbE/ Beta-Thalassaemia Patients in Malaysia

β-thalassaemia is a condition caused by the quantitative reduction or absence of β-globin chain synthesis due to β-globin gene mutations. It leads to excessive unpaired α-globin chains precipitates which causes membrane damage and ineffective erythropoiesis. Haemoglobin /β-thalassaemia patients have...

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Bibliographic Details
Main Author: Lim, Wai Feng
Format: Thesis
Language:English
Published: 2011
Subjects:
Online Access:http://psasir.upm.edu.my/id/eprint/21439/1/FPSK%28m%29_2011_22R.pdf
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