Polymorphic pattern of the (AT)x(T)y motif at −530 5′ to the β-globin gene in over 40 patients homozygous for various β-thalassemia mutations
Author:
Publisher
Wiley
Subject
Hematology
Reference30 articles.
1. The silent carrier allele: β thalassemia without a mutation in the β-globin gene or its immediate flanking regions
2. A beta-thalassemia carrier with normal sequence within the beta-globin gene [letter]
3. DNA sequence variation in a negative control region 5' to the beta- globin gene correlates with the phenotypic expression of the beta s mutation
4. Genetic epidemiology of β-thalassemia in sicily: Do sequences 5′ to theGγ gene and 5′ to the β gene interact to enhance HbF expression in β-thalassemia?
5. Increased protein binding to a −530 mutation of the human β-globin gene associated with decreased β-globin synthesis
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1. Genotype – Phenotype Correlations of β-Thalassemia Mutations in Azerbaijani population;Turkish Journal of Hematology;2017
2. Effect of a group of genetic markers around the 5′ regulatory regions of the β globin gene cluster linked to high HbF on the clinical severity of β thalassemia;Blood Cells, Molecules, and Diseases;2013-03
3. EFFECT OF CIS ACTING POTENTIAL REGULATORS IN THE ß GLOBIN GENE CLUSTER ON THE PRODUCTION OF HBF IN THALASSEMIA PATIENTS;Mediterranean Journal of Hematology and Infectious Diseases;2013-02-16
4. Association of polymorphic pattern of the (AT) × (T)y motif of β-globin gene in North Indian thalassemia patients with variable clinical expression;Indian Journal of Hematology and Blood Transfusion;2010-03
5. Human Hemoglobin;Vogel and Motulsky's Human Genetics;2010
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