Identification of a novel termination codon mutation (TAA-->TAT, Term-- >Tyr) in the alpha 2 globin gene of a Laotian girl with hemoglobin H disease [letter]
Author:
Publisher
American Society of Hematology
Subject
Cell Biology,Hematology,Immunology,Biochemistry
Link
http://ashpublications.org/blood/article-pdf/83/11/3418/613160/3418.pdf
Cited by 25 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 prevalence of thalassemia and hemoglobinopathies among the Lao Loum Group in the Lao People’s Democratic Republic;International Journal of Laboratory Hematology;2019-07-04
2. CODON 30 (–GAG) (α2): Hematological Parameters in Heterozygotes and also Patients with Hb H Disease;Hemoglobin;2013-07-04
3. Detection of Coinherited Hb H-Constant Spring/Paksé Disease and Hb E by Capillary Electrophoresis and High Performance Liquid Chromatography;Hemoglobin;2012-12-13
4. Unmasking Hb Paksé (codon 142, TAA>TAT,α2) and its Combinations in Patients also Carrying Hb Constant Spring (codon 142,TAA>CAA,α2) in Northern Thailand;Hemoglobin;2012-06
5. Molecular Screening of the Hbs Constant Spring (codon 142,TAA>CAA, α2) and PAKSÉ (codon 142, TAA>TAT, α2) Mutations in Thailand;Hemoglobin;2010-11-15
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