A mild form of Hb S-β-thalassemia syndrome is assured in Sicilian patients by β+mutant IVS-I nt 6(T→C)
Author:
Publisher
Wiley
Subject
Hematology,General Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1600-0609.1997.tb01412.x/fullpdf
Reference13 articles.
1. Molecular characterization of Hb S(C) β-thalassemia in American blacks;Gonzales-Redondo;Am J Hematol,1991
2. β-Thalassemia mutations in Mediterranean populations;Cao;Br J Haematol,1989
3. Genetic heterogeneity of β-thalassemia in Southeast Sicily;Schiliro';Am J Hematol,1995
4. Severity of β-thalassemia due to genotypes involving the IVS-I-6 (T→C) mutation;Waye;Am J Hematol,1995
5. Presence of hemoglobinopathies in Sicily: an historic perspective;Schiliro';Am J Med Genet,1996
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