Genetic studies suggest a multicentric origin for Hb G-coushatta [β22(B4)Glu→Ala]-Reference-Cited by-同舟云学术

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Genetic studies suggest a multicentric origin for Hb G-coushatta [β22(B4)Glu→Ala]

Published:1999-01 Issue:1 Volume:23 Page:57-67
ISSN:0363-0269
Container-title:Hemoglobin
language:en
Short-container-title:Hemoglobin

Author:

Li J.,Wilson D.,Plonczynski M.,Harrell A.,Cook C. B.,Scheer W. D.,Zeng Y-T.,Coleman M. B.,Steinberg M. H.

Publisher

Informa UK Limited

Subject

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

Link

http://www.tandfonline.com/doi/pdf/10.3109/03630269908996148

Reference40 articles.

1. Linkage of β-thalassaemia mutations and β-globin gene polymorphisms with DNA polymorphisms in human β-globin gene cluster

2. Polymorphism of DNA sequence adjacent to human beta-globin structural gene: relationship to sickle mutation.

3. Evidence for the multicentric origin of the sickle cell hemoglobin gene in Africa.

Cited by 6 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. Estimating the age of Hb G-Coushatta [β22(B4)Glu→Ala] mutation by haplotypes of β-globin gene cluster in Denizli, Turkey;Molecular Genetics & Genomic Medicine;2018-05-01

2. Molecular Studies on the Origin of the Hb G-Coushatta Mutation in Denizli Province of Turkey;Biochemical Genetics;2012-09-23

3. Further Identification of Hb G-Coushatta [β22(B4)Glu→Ala (GAA→GCA)] in Thailand by the Polymerase Chain Reaction-Single-Strand Conformation Polymorphism Technique and by Amplification Refractory Mutation System-Polymerase Chain Reaction;Hemoglobin;2007-01

4. Prevalence of the Sickle Cell Gene in Yemen: A Pilot Study;Hemoglobin;2004-01

5. Hb Siam [α1S(A13)Gly→Arg] is a GGT→CGT Mutation in the α1-Globin Gene;Hemoglobin;2000-01

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