A Rare Case of Alpha-Thalassaemia Intermedia in a Malay patient double heterozygous for a+-Thalassaemia and a mutation in a1 Globin Gene CD59 (GGC GAC)

George, E. and Tan, J. and Azian, A.S.N. and Rahimah, A. and Zubaidah, Z. (2009) A Rare Case of Alpha-Thalassaemia Intermedia in a Malay patient double heterozygous for a+-Thalassaemia and a mutation in a1 Globin Gene CD59 (GGC GAC). Medical Journal of Malaysia, 64 (4). p. 321. ISSN 0300-5283,

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Abstract

A rare case of thalassaemia-intermedia involving a nondeletion 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 establish the diagnosis.

Item Type: Article
Funders: UNSPECIFIED
Additional Information: Department of Molecular Medicine, Faculty of Medicine Building, University of Malaya, 50603 Kuala Lumpur, MALAYSIA
Uncontrolled Keywords: Alpha-thalassaemia intermedia, Non-deletion α1 globin gene CD59, Deletion -α 3.7, HPLC, Molecular analysis.
Subjects: R Medicine
Divisions: Faculty of Medicine
Depositing User: Ms Haslinda Lahuddin
Date Deposited: 01 Oct 2012 03:41
Last Modified: 26 Oct 2018 04:23
URI: http://eprints.um.edu.my/id/eprint/3714

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