Molecular characterisation of alpha-thalassaemia in patients investigated for hypochromic microcytic indices in Hospital Universiti Sains Malaysia

Alpha (α)-thalassaemia is a common genetic disorder that affects 5 % of the worldwide population. Deletional or non-deletional mutations of one or both HBA1 and HBA2 on chromosome 16 cause a reduction/abnormal in the production of α globin chains, a component of haemoglobin (Hb) which are require...

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Bibliographic Details
Main Author:	Vijian, Divashini
Format:	Thesis
Language:	English
Published:	2023
Subjects:	RC31-1245 Internal medicine
Online Access:	http://eprints.usm.my/58801/
Abstract	Abstract here

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