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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| Format: | Monograph |
| Language: | English |
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Universiti Sains Malaysia
2016
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| Online Access: | http://eprints.usm.my/62372/ http://eprints.usm.my/62372/1/NURUL%20ATIKAH%20BINTI%20RUSLI%20-%20e.pdf |