PMID: 3754242Jan 1, 1986Paper

Interaction of hemoglobin Siriraj with hemoglobin S: a mild sickle cell syndrome

Hemoglobin
M D RhodaF Galacteros

Abstract

Hb Siriraj is a beta chain variant in which beta 7 (A4) Glu is replaced by a lysine. It has been encountered in association with Hb S in a black man from Martinique. Some properties of Hb Siriraj are compared, particularly, with Hb C [alpha 2 beta 26(A3)Glu----Lys], and a study of its in vitro interaction with Hb S is discussed.

References

Feb 1, 1979·Proceedings of the National Academy of Sciences of the United States of America·R L NagelK Matsutomo
Aug 21, 1975·Nature·R M BookchinT Balazs
Nov 1, 1972·British Journal of Haematology·R W Carrell, R Kay
May 1, 1970·Analytical Biochemistry·Z B Rose, J Liebowitz
Dec 1, 1983·Nature·H F Bunn, M J McDonald
Aug 1, 1980·European Journal of Biochemistry·J FöldiJ Rosa
Feb 28, 1980·Nature·R L NagelO Castro
Dec 12, 1959·Nature·K BETKEI SCHLICHT
Jun 19, 1965·British Medical Journal·S TUCHINDAH LEHMANN

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Citations

Jan 1, 1989·Hemoglobin·J FöldiB V Rozynov
Oct 13, 2009·Nutrition·Alaa Al-KhalifaHussein M Dashti

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