Clinico-haematological profiling of transfusion dependent and non transfucion dependent beta thalassaemia syndrome in Kedah
Introduction: β thalassaemia is a group of haemoglobin diseases caused by a reduction or absence in the synthesis of β globin chains. Affected individuals can be heterozygous, compound heterozygous, or homozygous for β thalassaemia, or even have interactions with other haemoglobinopathies. Kedah has...
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| Format: | Thesis |
| Language: | English |
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2020
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| Online Access: | http://eprints.usm.my/49359/1/Fahmaa%20Azizi-24%20pages.pdf http://eprints.usm.my/49359/ |
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