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: | Thèse |
| Langue: | anglais |
| Publié: |
2020
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| Accès en ligne: | http://eprints.usm.my/49359/ |
| Abstract | Abstract here |