Molecular basis of alpha thalassemia among aborigines
in Kelantan

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Molecular basis of alpha thalassemia among aborigines in Kelantan

Alpha thalassemia is a common inherited disorder of hemoglobin (Hb) synthesis throughout all tropical and subtropical regions of the world. It is normally results from deletion of one or both alpha genes at chromosomes 16pl 3.3. Carriers of these genes have a variable degree of anemia (low Hb), de...

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Bibliographic Details
Main Author:	Rusli, Nurul Atikah
Format:	Monograph
Language:	English
Published:	Universiti Sains Malaysia 2016
Subjects:	R Medicine (General) RC Internal medicine
Online Access:	http://eprints.usm.my/62372/ http://eprints.usm.my/62372/1/NURUL%20ATIKAH%20BINTI%20RUSLI%20-%20e.pdf

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