Xmn I polymorphism in Egyptian patients with β-thalassemia major and its correlation with the HbF level
Author:
Publisher
Elsevier BV
Subject
Genetics
Reference21 articles.
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2. Variable severityof β-thalassaemia patients of Eastern India: effect of α-thalassaemia and XmnI polymorphism;Bandyopadhyay;Clin. Exp. Med.,2001
3. Hb F production in β thalassemia heterozygotes for the β0 IVS II-1 (G > A) globin mutation implication of the haplotype and the Gγ-158 (C > T) mutation on the Hb F level;Dedoussis;Am. J. Hematol.,2000
4. New insights on β-thalassemia in the palestinian population of Gaza: high frequency and milder phenotype among homozygous IVS-I-1 (HBB: c.92 + 1G > A) patients with high levels of Hb F;Hussam;Hemoglobin,2017
5. Foetal haemoglobin and disease severity in sickle cell anaemia patients in Kampala, Uganda;Mpalampa;BMC Blood Disord.,2012
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1. Association Between Selected Single Nucleotide Polymorphisms in Globin and Related Genes and Response to Hydroxyurea Therapy in Ghanaian Children with Sickle Cell Disease;Pharmacogenomics and Personalized Medicine;2022-03
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