Two New α-Thalassemia Frameshift Mutations-Reference-Cited by-同舟云学术

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Two New α-Thalassemia Frameshift Mutations

Published:2007-01 Issue:2 Volume:31 Page:135-139
ISSN:0363-0269
Container-title:Hemoglobin
language:en
Short-container-title:Hemoglobin

Author:

Luo Hong-Yuang,Adewoye Adeboye H.,Pilichowska Monika,Li Michael Yunlong,Basran Raveen K.,Steinberg Martin H.,Chui David H.K.

Publisher

Informa UK Limited

Subject

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

Link

http://www.tandfonline.com/doi/pdf/10.1080/03630260701285118

Reference6 articles.

1. Three New α-Thalassemia Point Mutations Ascertained Through Newborn Screening

2. Hemoglobinopathies mimicking Hb S/β-thalassemia: Hb S/S with α-thalassemia and Hb S/Volga

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

4. Nonsense-mediated mRNA decay in mammals

Cited by 5 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. α-Thalassemia Trait Caused by Frameshift Mutations in Exon 2 of theα2-Globin Gene: HBA2:c.131delT and HBA2:c.143delA;Hemoglobin;2012-06

2. Secondary Mutation (c.94_95delAG) in A −α3.7Allele Associated with Hb H Disease in Two Unrelated African American Individuals Homozygous for the −α3.7Deletion (−α3.7/−α3.7T);Hemoglobin;2011-12-21

3. Two New α-Thalassemia Point Mutations that are Undetectable by Biochemical Techniques;Hemoglobin;2008-01

4. Frameshift Mutation in the α2-Globin Gene Causing α+-Thalassemia: Codon 49 (−GC);Hemoglobin;2008-01

5. Sickle Cell Trait;Disorders of Hemoglobin

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