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Hemoglobin
international journal for hemoglobin research
Volume 23, 1999 - Issue 1
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BriefNote Article

Hb G-coushatta [β22(B4)Glu→Ala] in Thailand

D. Itchayanan Department of Biochemistry, Faculty of Science, Mahidol University, Bangkok, 10400, ThailandView further author information
,
J. Svasti Department of Biochemistry, Faculty of Science, Mahidol University, Bangkok, 10400, Thailand; Laboratory of Biochemistry,Chulabhorn Research Institute, Bangkok, 10210, ThailandCorrespondence[email protected]
,
C. Srisomsap Laboratory of Biochemistry,Chulabhorn Research Institute, Bangkok, 10210, Thailand
,
P. Winichagoon The Thalassemia Center Institute of Science and Technology for Research and Development Mahidol University, Salaya, Nakorn Pathom, 73170, Thailand
&
S. Fucharoen The Thalassemia Center Institute of Science and Technology for Research and Development Mahidol University, Salaya, Nakorn Pathom, 73170, Thailand
Pages 69-72 | Received 26 Jun 1998, Accepted 26 Aug 1998, Published online: 05 Aug 2009

Citations (9)

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Worrawut Chinchang & Vip Viprakasit. (2007) 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 31:1, pages 93-99.
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Lukana Ngiwsara, Chantragan Srisomsap, Pranee Winichagoon, Suthat Fucharoen & Jisnuson Svasti. (2003) Hb Kodaira II [β146(HC3)His→Gln] Detected in Thailand. Hemoglobin 27:1, pages 37-39.
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Phannee Sawangareetrakul, Saovaros Svasti, Boonpa Yodsowon, Pranee Winichagoon, Chantragan Srisomsap, Jisnuson Svasti & Suthat Fucharoen. (2002) DOUBLE HETEROZYGOSITY FOR Hb PYRGOS [β83(EF7)Gly→Asp] AND Hb E [β26(B8)Glu→Lys] FOUND IN ASSOCIATION WITH α-THALASSEMIA. Hemoglobin 26:2, pages 191-196.
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Saovaros Svasti, Boonpa Yodsowon, Roongrat Sriphanich, Pranee Winichagoon, Pattraporn Boonkhan, Tawatchai Suwanban, Phannee Sawangareetrakul, Chantragan Srisomsap, James R. Ketudat-Cairns, Jisnuson Svasti & Suthat Fucharoen. (2001) ASSOCIATION OF Hb HOPE [β136(H14)Gly → Asp] AND Hb H DISEASE. Hemoglobin 25:4, pages 429-435.
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B. Yodsowan, J. Svasti, C. Srisomsap, P. Winichagoon & S. Fucharoen. (2000) Hb Siam [α1S(A13)Gly→Arg] is a GGT→CGT Mutation in the α1-Globin Gene. Hemoglobin 24:1, pages 71-75.
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Articles from other publishers (4)

Narges Soozangar, Ehsan Abbaspour, Haleh Mokaber, Zahra Nematollahi & Behzad Davarnia. (2023) A novel compound heterozygous of β-thalassemia with HbG-Coushatta: case report of Iran. Human Genome Variation 10:1.
Crossref
Onur Ozturk, Sanem Arikan, Ayfer Atalay & Erol O. Atalay. (2018) 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 6:4, pages 547-554.
Crossref
Martin H. Steinberg, Bernard G. Forget, Douglas R. Higgs & David J. WeatherallMartin H. Steinberg & Ronald L. Nagel. 2010. Disorders of Hemoglobin. Disorders of Hemoglobin 589 606 .
Martin H. Steinberg, Bernard G. Forget, Douglas R. Higgs & David J. WeatherallMartin H. Steinberg. 2010. Disorders of Hemoglobin. Disorders of Hemoglobin 587 588 .

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