The β-globin C→G mutation at 6 bp 3′ to the termination codon causes β-thalassaemia by decreasing the mRNA level
Author:
Publisher
Wiley
Subject
Hematology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1046/j.1365-2141.2002.03627.x/fullpdf
Reference29 articles.
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2. DNA haplotype heterogeneity of β-thalassaemia in Greece: feasibility of prenatal diagnosis;Athanassiadou;British Journal of Haematology,1987
3. A novel 13bp deletion in the 3′UTR of the beta-globin gene causes beta-thalassaemia in a Turkish patient;Basak;Hemoglobin,1993
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