α-Thalassemia Trait Caused by Frameshift Mutations in Exon 2 of theα2-Globin Gene: HBA2:c.131delT and HBA2:c.143delA-Reference-Cited by-同舟云学术

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α-Thalassemia Trait Caused by Frameshift Mutations in Exon 2 of theα2-Globin Gene: HBA2:c.131delT and HBA2:c.143delA

Published:2012-06 Issue:5 Volume:36 Page:511-515
ISSN:0363-0269
Container-title:Hemoglobin
language:en
Short-container-title:Hemoglobin

Author:

Finlayson Jill,Ghassemifar Reza,Holmes Paula,Grey Dianne,Newbound Christopher,Pell Nicole,Jennens Michelle,Greenwood Laura,Beilby John

Publisher

Informa UK Limited

Subject

Biochemistry (medical),Clinical Biochemistry,Genetics (clinical),Hematology

Link

http://www.tandfonline.com/doi/pdf/10.3109/03630269.2012.717053

Reference7 articles.

1. A rapid and reliable 7-deletion multiplex polymerase chain reaction assay for α-thalassemia

2. Molecular basis for nondeletion alpha-thalassemia in American blacks. Alpha 2(116GAG----UAG).

3. NMD: RNA biology meets human genetic medicine

4. Human alpha2-globin nonsense-mediated mRNA decay induced by a novel alpha-thalassaemia frameshift mutation at codon 22

5. Two New α-Thalassemia Frameshift Mutations

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. Hemoglobinopathy gone astray—three novel forms of α-thalassemia in Norwegian patients characterized by quantitative real-time PCR and DNA sequencing;Scandinavian Journal of Clinical and Laboratory Investigation;2021-11-18

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