A rare case of alpha-thalassaemia intermedia in a Malay patient double heterozygous for α+ –thalassaemia and a mutation in α1 globin gene CD59 (GGC → GAC)
A rare case of thalassaemia-intermedia involving a non-deletion alpha thalassemia point mutation in the α1-globin gene CD59 (GGC → GAC) and a deletion α+ (-α3.7) thalassaemia in which use of high performance liquid chromatography (HPLC) C-gram Hb subtype profile and DNA molecular analysis helped est...
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| Main Authors: | , , , , |
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| Format: | Article |
| Language: | English |
| Published: |
Malaysian Medical Association
2009
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| Online Access: | http://psasir.upm.edu.my/id/eprint/12806/1/A%20rare%20case%20of%20alpha-thalassaemia%20intermedia%20in%20a%20Malay%20patient%20double%20heterozygous%20for%20%CE%B1%2B%20%E2%80%93thalassaemia%20and%20a%20mutation%20in%20%CE%B11%20globin%20gene%20CD59%20%28GGC%20%E2%86%92%20GAC%29.pdf http://psasir.upm.edu.my/id/eprint/12806/ http://www.e-mjm.org/2009/v64n4/index.html |
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http://psasir.upm.edu.my/id/eprint/12806/1/A%20rare%20case%20of%20alpha-thalassaemia%20intermedia%20in%20a%20Malay%20patient%20double%20heterozygous%20for%20%CE%B1%2B%20%E2%80%93thalassaemia%20and%20a%20mutation%20in%20%CE%B11%20globin%20gene%20CD59%20%28GGC%20%E2%86%92%20GAC%29.pdfhttp://psasir.upm.edu.my/id/eprint/12806/
http://www.e-mjm.org/2009/v64n4/index.html