The 12.6 kb-deletion in the β-globin gene cluster is the known Thai/Vietnamese (δβ)0-thalassemia commonly found in Southeast Asia.
作者信息
Chalaow Nipon, Thein Swee Lay, Viprakasit Vip
出版信息
Haematologica. 2013 Sep;98(9):e117-8. doi: 10.3324/haematol.2013.090613.
Abstract
摘要
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The 12.6 kb-deletion in the β-globin gene cluster is the known Thai/Vietnamese (δβ)0-thalassemia commonly found in Southeast Asia.
Haematologica. 2013 Sep;98(9):e117-8. doi: 10.3324/haematol.2013.090613.
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Low fetal hemoglobin rates in patients carrying Thai (δβ)0-deletion and Turkish (δβ)0-deletion/inversion strengthen the hypothesis that the 5'δ BCL11A binding site plays a major role in its fetal hemoglobin inhibitory regulation. Response to "The 12.6 kb-deletion in the β-globin gene cluster is the known Thai/Vietnamese (δβ)0-thalassemia commonly found in Southeast Asia".
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Low fetal hemoglobin rates in patients carrying Thai (δβ)0-deletion and Turkish (δβ)0-deletion/inversion strengthen the hypothesis that the 5'δ BCL11A binding site plays a major role in its fetal hemoglobin inhibitory regulation. Response to "The 12.6 kb-deletion in the β-globin gene cluster is the known Thai/Vietnamese (δβ)0-thalassemia commonly found in Southeast Asia".
Haematologica. 2013 Sep;98(9):e119-20. doi: 10.3324/haematol.2013.093716.
本文引用的文献
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A single-tube multiplex gap-polymerase chain reaction for the detection of eight β-globin gene cluster deletions common in Southeast Asia.
Hemoglobin. 2012;36(6):571-80. doi: 10.3109/03630269.2012.747441.
2
Estimation of the difference in HbF expression due to loss of the 5' δ-globin BCL11A binding region.
Haematologica. 2013 Feb;98(2):305-8. doi: 10.3324/haematol.2012.061994. Epub 2012 Jul 16.
3
Large-scale population genetic analysis for hemoglobinopathies reveals different mutation spectra in central Greece compared to the rest of the country.
Am J Hematol. 2007 Jul;82(7):634-6. doi: 10.1002/ajh.20889.
4
Molecular characterization of (deltabeta)(0)/beta(0)-thalassemia and (deltabeta)(0)-thalassemia/hemoglobin E in Thai patients.
Eur J Haematol. 2001 Oct;67(4):258-62. doi: 10.1034/j.1600-0609.2001.00524.x.
5
Molecular analysis of the Turkish form of deletion-inversion (delta beta)(0) thalassaemia.
Br J Haematol. 1997 Feb;96(2):229-34. doi: 10.1046/j.1365-2141.1997.d01-2022.x.
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7
8
Thai (delta beta)0-thalassemia and its interaction with gamma-thalassemia.
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