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Hemoglobin
international journal for hemoglobin research
Volume 40, 2016 - Issue 4
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Short Communication

A Novel Mutation in the Promoter Region of the β-Globin Gene: HBB: c.-127G > C

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Pages 280-282 | Received 07 Mar 2016, Accepted 12 May 2016, Published online: 28 Jun 2016

References

  • Trent RJ. Diagnosis of the haemoglobinopathies. Clin Biochem Rev. 2006:27(1):27–38
  • Patrinos GP, Wajcman H. Recording human globin gene variation. Hemoglobin. 2004;28(2):v–vii
  • Uda M, Galanello R, Sanna S, et al. Genome-wide association study shows BCL11A associated with persistent fetal hemoglobin and amelioration of the phenotype of β-thalassemia. Proc Natl Acad Sci USA. 2008;105(5):1620–1625
  • Sollaino MC, Paglietti ME, Perseu L, et al. Association of α globin gene quadruplication and heterozygous β thalassemia in patients with thalassemia intermedia. Haematologica. 2009;94(10):1445–1448
  • Galanello R, Cao A. Relationship between genotype and phenotype. Thalassemia intermedia. Ann N Y Acad Sci. 1998;850:325–333
  • Rosatelli C, Leoni GB, Tuveri T, et al. Heterozygous β-thalassemia: Relationship between the hematological phenotype and the type of β-thalassemia mutation. Am J Hematol. 1992;39(1):1–4
  • Danjou F, Anni F, Galanello R. β-Thalassemia: From genotype to phenotype. Haematologica. 2011;96(11):1573–1575

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