Molecular characterization of a novel 10.3 kb deletion causing β-thalassaemia with unusually high Hb A2
Author:
Publisher
Wiley
Subject
Hematology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2141.1992.tb06952.x/fullpdf
Reference36 articles.
1. Hemoglobin A2 in health and various hematologic disorders;Alperin;American Journal of Clinical Pathology,1977
2. Gene analysis of δβ and δ thalassemia;Baird;Journal of Biological Chemistry,1984
3. Human γ- to β-globin gene switching in transgenic mice;Behringer;Genes and Development,1990
4. Observations on the levels of Hb A2 in patients with different β-thalassemia mutations and a δ chain variant;Codrington;Blood,1990
5. An ∼ 300 bp deletion involving part of the 5′β-globin gene region is observed in members of a Turkish family with β-thalassemia;Diaz-Chico;Blood,1987
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2. Disrupting the adult globin promoter alleviates promoter competition and reactivates fetal globin gene expression;Blood;2022-04-07
3. A rare complex rearrangement in the β‐globin gene cluster causing a novel homozygous G γ( A γδβ) 0 ‐thalassemia;American Journal of Hematology;2021-03-22
4. Whole genome sequence-based haplotypes reveal a single origin of the 1393 bp HBB deletion;Journal of Medical Genetics;2020-01-30
5. Molecular basis of β thalassemia and potential therapeutic targets;Blood Cells, Molecules, and Diseases;2018-05
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