Combination of two rare mutations causes β-thalassaemia in a Bangladeshi patient
Author:
Affiliation:
1. University of Dhaka, Bangladesh
2. Dhaka Shishu Hospital, Bangladesh
Publisher
FapUNIFESP (SciELO)
Subject
Genetics,Molecular Biology
Link
http://www.scielo.br/pdf/gmb/v34n3/2011-064.pdf
Reference30 articles.
1. Oxidative status of platelets in normal and thalassemic blood;Amer J;Thromb Haemost,2004
2. Identification of a beta-thalassemia mutation associated with a novel haplotype;Atweh GF;Am J Hum Genet,1986
3. Mutation analysis of HBB gene in selected Bangladeshi β thalassemic individuals: Presence of rare mutations;Ayub MI;Genet Test Mol Biomarkers,2010
4. Variable severity of α-thalassemia patients of Eastern India: Effect of β-thalassemia and XmnI polymorphism;Bandyopadhyay S;Clin Exp Med,2001
5. DNAzol: A reagent for the rapid isolation of genomic DNA;Chomczynski P;Biotechniques,1997
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