Haemoglobin Adana in alpha thalassaemia intermedia in the Malaysian population

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Haemoglobin Adana in alpha thalassaemia intermedia in the Malaysian population

Alpha thalassaemia is an autosomal blood disorder due to a quantitative reduction or total absence of alpha globin chain synthesis caused by alpha globin gene mutations. Alpha thalassaemia intermedia or more commonly known as HbH disease is a form of thalassaemia with intermediate severity. A...

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Bibliographic Details
Main Author:	Lee, Tze Yan
Format:	Thesis
Language:	English
Published:	2017
Subjects:	Hemoglobins - biosynthesis Alpha-Thalassemia - drug therapy
Online Access:	http://psasir.upm.edu.my/id/eprint/69661/ http://psasir.upm.edu.my/id/eprint/69661/1/fpsk%202017%2021%20ir.pdf

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