Molecular Characterisation of Alpha-Thalassaemia in Patients Investigated for Hypochromic Microcytic Indices in Hospital Universiti Sains Malaysia

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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書目詳細資料
主要作者:	Vijian, Divashini
格式:	Thesis
語言:	English
出版:	2023
主題:	RC31-1245 Internal medicine
在線閱讀:	http://eprints.usm.my/58801/1/03-DIVASHINI%20AP%20VIJIAN-FINAL%20THESIS%20P-SGM000820%28R%29-24%20pages.pdf
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