Nucleotide −88 (C-T) promoter mutation is a common β-thalassemia mutation in the Jat Sikhs of Punjab, India

Author:

Garewal Gurjeewan,Das Reena,Ahluwalia Jasmina,Marwaha R.K.,Varma S.

Publisher

Wiley

Subject

Hematology

Reference17 articles.

1. Clinical and genetic heterogeneity in black patients with homozygous beta-thalassemia from the southeastern United States

2. Base substitution at position -88 in a beta-thalassemic globin gene. Further evidence for the role of distal promoter element ACACCC.

3. Regional distribution of β-thalassemia mutations in India

4. DNA-based diagnosis of the hemoglobin disorders. In: , , , , editors. Disorders of haemoglobin: genetics, pathophysiology and clinical management. Cambridge, England: Cambridge University Press; 2001. 947 p.

5. , , , Thalassaemia intermedia. In: , , editors. The thalassaemia syndromes, 4th edition. Oxford, England: Blackwell Science; 2001. 555 p.

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