Haemoglobin Adana in alpha thalassaemia intermedia in the Malaysian population
Alpha thalassaemia is an autosomal blood disorder due to a quantitative reduction or total absence of alpha globin chain synthesis caused by alpha globin gene mutations. Alpha thalassaemia intermedia or more commonly known as HbH disease is a form of thalassaemia with intermediate severity. A...
| Príomhchruthaitheoir: | |
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| Formáid: | Tráchtas |
| Teanga: | English |
| Foilsithe / Cruthaithe: |
2017
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| Ábhair: | |
| Rochtain ar líne: | http://psasir.upm.edu.my/id/eprint/69661/1/fpsk%202017%2021%20ir.pdf |