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-Reference-Cited by-同舟云学术

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

Published:2007-01 Issue:1 Volume:31 Page:93-99
ISSN:0363-0269
Container-title:Hemoglobin
language:en
Short-container-title:Hemoglobin

Author:

Chinchang Worrawut,Viprakasit Vip

Publisher

Informa UK Limited

Subject

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

Link

http://www.tandfonline.com/doi/pdf/10.1080/03630260601059225

Reference20 articles.

1. Hemoglobin G coushatta : A New Variant in an American Indian Family

2. HEMOGLOBIN G SASKATOON: β22Glu → Ala

3. Hemoglobin Variant Common to Chinese and North American Indians: α 2 β 2 22Glu→Ala

4. Hemoglobin Variants in Koreans: Hemoglobin G Taegu

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

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1. A novel compound heterozygous of β-thalassemia with HbG-Coushatta: case report of Iran;Human Genome Variation;2023-05-15

2. 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

3. Interaction between Hb E and Hb Yala (HBB:c.129delT); a novel frameshift beta globin gene mutation, resulting in Hemoglobin E/β0 thalassemia;Hematology;2017-08-03

4. Two rare hemoglobin variants in the Cukurova Region of Turkey: Hb E-Saskatoon and Hb G-Coushatta;Turkish Journal of Hematology;2011-12-01

5. Toward a fluorescent single-strand conformation polymorphism technique that detects all mutations: F-DOVAM-S;Analytical Biochemistry;2007-09