Hb G-coushatta [β22(B4)Glu→Ala] in Thailand
Author:
Publisher
Informa UK Limited
Subject
Biochemistry (medical),Clinical Biochemistry,Genetics (clinical),Hematology
Link
http://www.tandfonline.com/doi/pdf/10.3109/03630269908996149
Reference13 articles.
1. Hemoglobin GCoushatta: A beta variant with a delta-like substitution
2. HEMOGLOBIN G SASKATOON: β22Glu → Ala
3. Hemoglobin Variant Common to Chinese and North American Indians: α 2 β 2 22Glu→Ala
4. Hemoglobin variant found in Koreans, Chinese, and North American Indians: α2β222glu→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. Two rare hemoglobin variants in the Cukurova Region of Turkey: Hb E-Saskatoon and Hb G-Coushatta;Turkish Journal of Hematology;2011-12-01
4. 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
5. Hb Kodaira II [β146(HC3)His→Gln] Detected in Thailand;Hemoglobin;2003-01
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