First Identification of a Point Mutation at Position −83 (G>A) of the β-Globin Gene Promoter
Author:
Publisher
Informa UK Limited
Subject
Biochemistry, medical,Clinical Biochemistry,Genetics(clinical),Hematology
Link
http://www.tandfonline.com/doi/pdf/10.1080/03630260903081323
Reference17 articles.
1. Disorders of Hemoglobin Structure and Synthesis
2. The Thalassaemia Syndromes
3. A Novel β-Thalassemic Allele Due to a Two Nucleotide Deletion: β76 (−GC)
4. Identification of four novel delta-globin gene mutations in Greek Cypriots using polymerase chain reaction and automated fluorescence- based DNA sequence analysis
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1. The Effect of HBB: c.-121C>T Variant [–71 (C>T)] on the β-Globin Promoter: Case Series Study;Hemoglobin;2021-07-04
2. Borderline HbA2 levels: Dilemma in diagnosis of beta-thalassemia carriers;Mutation Research/Reviews in Mutation Research;2021-07
3. The regulation of human globin promoters by CCAAT box elements and the recruitment of NF-Y;Biochimica et Biophysica Acta (BBA) - Gene Regulatory Mechanisms;2017-05
4. Two new β+-thalassemia mutation [β -56 (G → C); HBBc. −106 G → C] and [β −83 (G → A); HBBc. −133 G → A] described among the Tunisian population;American Journal of Human Biology;2015-03-07
5. Non-Thalassemic Phenotype Associated With the -83 (G > A) Mutation of theβ-Globin Gene Promoter (HBB: c.-133G > A);Hemoglobin;2014-11-18
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