Nonsense mutation of β-globin gene at codon 82 (AAG→TAG) or HBB:C247 A→T with polymorphism: cause of thalassemia intermedia?-Reference-Cited by-同舟云学术

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Nonsense mutation of β-globin gene at codon 82 (AAG→TAG) or HBB:C247 A→T with polymorphism: cause of thalassemia intermedia?

Published:2010-11-04 Issue:2 Volume:33 Page:e3-e4
ISSN:1751-5521
Container-title:International Journal of Laboratory Hematology
language:en
Short-container-title:

Author:

Kumar R.,Agarwal S.

Publisher

Wiley

Subject

Biochemistry, medical,Clinical Biochemistry,Hematology,General Medicine

Reference7 articles.

1. Prenatal diagnosis in beta thalassemia: an Indian experience;Agarwal;Fetal Diagnosis and Therapy,2003

2. Clinical and haematological features in a compound heterozygote (HBB:c.92 + 5G > C/HBB:c.93-2A > C) case of thalassaemia major;Agarwal;International Journal of Laboratory Hematology,2010

3. A novel homozygous point mutation at codon 82 (HBB:c.247A > T)) in the beta-globin gene leads to thalassemia major;Angalena;International Journal of Laboratory Hematology,2010

4. Identification of the multiple β-thalassemia mutations by denaturing gradient gel electrophoresis;Cai;Journal of Clinical Investigation,1990

5. Molecular analysis of unknown β-globin gene mutations using polymerase chain reaction-single strand conformation polymorphism (PCR-SSCP) technique and its application in Thai families with β-thalassemias and β-globin variants;Chinchang;Clinical Biochemistry,2005

Cited by 1 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Molecular Basis of β-Thalassemia in Karnataka, India;Genetic Testing and Molecular Biomarkers;2012-02

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