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: George, Elizabeth, Tan, Mary Anne Jin Ai, A. S., Nor Azian, Ahmad, Rahimah, Zakaria, Zubaidah
Format: Article
Language:English
Published: Malaysian Medical Association 2009
Online Access:http://psasir.upm.edu.my/id/eprint/12806/
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
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author George, Elizabeth
Tan, Mary Anne Jin Ai
A. S., Nor Azian
Ahmad, Rahimah
Zakaria, Zubaidah
author_facet George, Elizabeth
Tan, Mary Anne Jin Ai
A. S., Nor Azian
Ahmad, Rahimah
Zakaria, Zubaidah
author_sort George, Elizabeth
building UPM Institutional Repository
collection Online Access
description 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 establish the diagnosis.
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institution Universiti Putra Malaysia
institution_category Local University
language English
last_indexed 2025-11-15T07:51:09Z
publishDate 2009
publisher Malaysian Medical Association
recordtype eprints
repository_type Digital Repository
spelling upm-128062016-11-30T03:07:22Z http://psasir.upm.edu.my/id/eprint/12806/ 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) George, Elizabeth Tan, Mary Anne Jin Ai A. S., Nor Azian Ahmad, Rahimah Zakaria, Zubaidah 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 establish the diagnosis. Malaysian Medical Association 2009-12 Article PeerReviewed application/pdf en 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 George, Elizabeth and Tan, Mary Anne Jin Ai and A. S., Nor Azian and Ahmad, Rahimah and Zakaria, Zubaidah (2009) 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). Medical Journal of Malaysia, 64 (4). pp. 321-322. ISSN 0300-5283 http://www.e-mjm.org/2009/v64n4/index.html
spellingShingle George, Elizabeth
Tan, Mary Anne Jin Ai
A. S., Nor Azian
Ahmad, Rahimah
Zakaria, Zubaidah
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)
title 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)
title_full 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)
title_fullStr 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)
title_full_unstemmed 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)
title_short 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)
title_sort 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)
url http://psasir.upm.edu.my/id/eprint/12806/
http://psasir.upm.edu.my/id/eprint/12806/
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