Identification of a novel frameshift β-thalassemia mutation in an Asian Indian
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1034/j.1399-0004.2000.570412.x/fullpdf
Reference6 articles.
1. The β- and Δ-thalassemia repository (ninth edition);Baysal;Hemoglobin,1998
2. Construction of human gene libraries from small amounts of peripheral blood: analysis of beta-like globin genes;Poncz;Hemoglobin,1982
3. The spectrum of β-thalassemia mutations on the Indian subcontinent: the basis for prenatal diagnosis;Varawalla;Br J Haematol,1991
4. A new β-thalassemia allele, codon 26 (GAG-GTAG), found in a Japanese;Hattori;Hemoglobin,1998
5. The spectrum of β-thalassemia mutations in Taiwan: identification of novel frameshift mutation;Lin;Am J Hum Gent,1991
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1. Biochemical and molecular analysis of the beta-globin gene and LCR region on Saudi β-thalassemia patients;Saudi Journal of Biological Sciences;2020-11
2. A Novel 26 bp Deletion [HBB: c.20_45del26bp] in Exon 1 of the β-Globin Gene Causing β-Thalassemia Major;Hemoglobin;2012-01-10
3. Regional heterogeneity of β-thalassemia mutations in the multi ethnic Indian population;Blood Cells, Molecules, and Diseases;2009-05
4. Detection of Rare β‐Thalassemia Mutations by Denaturing Gradient Gel Electrophoresis Among Indians;Hemoglobin;2004-01
5. Rare ?-thalassemia mutations in Asian Indians;American Journal of Hematology;2000
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