LETTER TO THE EDITOR: A novel homozygous point mutation at codon 82 (HBB:c.247A > T) in the beta-globin gene leads to thalassemia major-Reference-Cited by-同舟云学术

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LETTER TO THE EDITOR: A novel homozygous point mutation at codon 82 (HBB:c.247A > T) in the beta-globin gene leads to thalassemia major

Published:2010-08-23 Issue:5 Volume:32 Page:548-549
ISSN:1751-5521
Container-title:International Journal of Laboratory Hematology
language:en
Short-container-title:

Author:

Angalena R.,Prabitha K. N.,Chaudhary A. K.,Bashyam M. D.,Jain S.,Dalal A. B.

Publisher

Wiley

Subject

Biochemistry, medical,Clinical Biochemistry,Hematology,General Medicine

Reference9 articles.

1. Detection of a rare beta-globin nonsense mutation [codon 59 (AAG → TAG)] in an Italian family;Amato;Hemoglobin,2006

2. Molecular genetic analyses of b-thalassemia in South India reveals rare mutations in the b-globin gene;Bashyam;Journal of Human Genetics,2004

3. Hb Lulu Island (alpha 2 beta 2 107[G9]Gly → Asp)-beta zero-thalassemia (codon 15; TGG → TAG), a form of thalassemia intermedia;Gray;American Journal of Hematology,1995

4. Beta O-39 thalassemia gene: a premature termination codon causes beta-mRNA deficiency without affecting cytoplasmic beta-mRNA stability;Humphries;Blood,1984

5. A novel beta-globin mutation (HBB:c.107A > G; or codon 35 beta (A → G)) at alpha-beta chain interfaces;Kumar;Annals of hematology,2009

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. Nonsense mutation of β-globin gene at codon 82 (AAG→TAG) or HBB:C247 A→T with polymorphism: cause of thalassemia intermedia?;International Journal of Laboratory Hematology;2010-11-04

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