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".
作者信息
Ghedira Elyes Slim, Pissard Serge
出版信息
Haematologica. 2013 Sep;98(9):e119-20. doi: 10.3324/haematol.2013.093716.
Abstract
摘要
相似文献
1
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.
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本文引用的文献
1
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.
2
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.
3
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.
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.
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Thai (delta beta)0-thalassemia and its interaction with gamma-thalassemia.
Hemoglobin. 1988;12(2):101-14. doi: 10.3109/03630268808998017.
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