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

Hemoglobin

Volumn 23, Issue 1, 1999, Pages 69-72

  Itchayanan, D ^a   Svasti, J ^a,b   Srisomsap, C ^b   Winichagoon, P ^a   Fucharoen, S ^a  

^a MAHIDOL UNIVERSITY   (Thailand)

^b Krung Thep Maha Nakhon   (Thailand)

Author keywords

[No Author keywords available]

Indexed keywords

ALANINE; GLUTAMIC ACID; HEMOGLOBIN VARIANT; UNCLASSIFIED DRUG;

ADULT; ARTICLE; CASE REPORT; DNA SEQUENCE; FEMALE; GENE MUTATION; GLOBIN GENE; HAPLOTYPE; HEMOGLOBIN DETERMINATION; HEMOGLOBIN G COUSHATTA; HUMAN; THAILAND;

EID: 0033024293     PISSN: 03630269     EISSN: None     Source Type: Journal    
DOI: 10.3109/03630269908996149     Document Type: Article

References (13)

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10. Winichagoon, P., Fucharoen, S., Thonglairoam, V., Tanapotiwirut, V. and Wasi, P.: β-Thalassemia in Thailand. Ann. N.Y. Acad. Sci., 612:31-43, 1990.
11. Siriboon, W., Svasti, M.R.J., Srisomsap, C., Winichagoon, P. and Fucharoen, S.: Discovery of a new Hemoglobin C mutation in Thailand. In: Biopolymers and Bioproducts: Structure, Function and Applications, edited by J. Svasti, V. Rimphanitchayakit, S. Soontaros, A. Tassanakajorn, T. Limpaseni, P. Pongsawasdi, P. Wilairat, B. Sonthayanon, J. Boonjawat, K. Packdibamrung, and S. Kamolsiripichaiporn, pages 159-163, Samakkhisan Public Co. Ltd., Bangkok, 1995.
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13. Wilson, D., Plonczynski, M., Harrell, A., Cook, C., Gorden, D., Scheer, W.D., Sekhon, B.S., Zeng, Y-T., Coleman, M.B., and Steinberg, M.H.: Genetic studies suggest multicentric origin for Hb G Coushatta. J. Invest. Med., 45:33a, 1997.