α+-Thalassemia Due to a Frameshift Mutation of theα2-Globin Gene [codons 55/56 (+T) orHBA2: c.168dup]-Reference-Cited by-同舟云学术

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α+-Thalassemia Due to a Frameshift Mutation of theα2-Globin Gene [codons 55/56 (+T) orHBA2: c.168dup]

Published:2015-04-21 Issue:3 Volume:39 Page:209-210
ISSN:0363-0269
Container-title:Hemoglobin
language:en
Short-container-title:Hemoglobin

Author:

Waye John S.,Eng Barry,Hanna Meredith,Hohenadel Betty-Ann,Nakamura Lisa M.,Walker Lynda

Publisher

Informa UK Limited

Subject

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

Link

http://www.tandfonline.com/doi/pdf/10.3109/03630269.2015.1030410

Reference9 articles.

1. The α-Thalassemias

2. Updates of the HbVar database of human hemoglobin variants and thalassemia mutations

3. Locus assignment of human a globin mutations by selective amplification and direct sequencing

4. Nonsense-mediated mRNA decay modulates clinical outcome of genetic disease

5. Novel Point Mutation of the α2-Globin Gene (HBA2) and a Rare 2.4 kb Deletion of the α1-Globin Gene (HBA1), Identified in Two Chinese Patients with Hb H Disease

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. Analysis of rare thalassemia genetic variants based on third-generation sequencing;Scientific Reports;2022-06-14

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