Association of polymorphic pattern of the (AT) × (T)y motif of β-globin gene in North Indian thalassemia patients with variable clinical expression
Author:
Publisher
Springer Science and Business Media LLC
Subject
Hematology
Link
http://link.springer.com/content/pdf/10.1007/s12288-010-0008-4.pdf
Reference8 articles.
1. Dimovski AJ, Adekile AD, Divoky V, Baysal E, Huisman THJ (1994) Polymorphic pattern of the (AT) × (T)y motif at −530 5′ to the β globin gène in over 40 homozygous for various β-thalassemia mutations. Am J Hematol 45:51–57
2. Berg PE, Williams DM, Quian RL, Cohen RB, Cao SX, Mittelman M, Schechter AN (1989) A common protein binds to two silencers 5′ to the human β-globin gene. Nucleic Acids Res 17:8833–8352
3. Agarwal S, Gupta UR, Gupta A, Sarwai S, Phadke S, Agarwal SS (2003) Prenatal diagnosis in β-thalassemia: An Indian experience. Fetal Diagnosis and Therapy 18:328–332
4. Gesperini D, Perseu L, Melis MA, Maccioni L, Sollaino MC, Paglietti E, Cao A, Galanello R (1998) Heterozygous β-thalassemia with thalassemia intermedia phenotype. Am J Hematol 57:43–47
5. Ferrara M, Matarese SMR, Francese M, Borrelli B, Perrotta A, Meo A, Rosa MAL, Esposito L (2003) Role of polymorphic séquences 5′ to the Gγ gène and 5′ to the β gene on the homozygous β-thalassemic phenotype. Hemoglobin 27(3):167–175
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1. The Influence of Polymorphisms in Disease Severity in β-Thalassemia;Biochemical Genetics;2015-07-05
2. Genotype–phenotype correlation and report of novel mutations in β-globin gene in thalassemia patients;Blood Cells, Molecules, and Diseases;2015-06
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
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