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CONTACT | |
Internal | |
HEMATOLOGY | |
Erythrocytosis in the heterozygote (PCV 0.62 l/l) | |
ELECTROPHORESIS | |
No separation of Hb X and Hb A | |
CHROMATOGRAPHY | |
No separation of Hb X and Hb A | |
STRUCTURE STUDIES | |
Tryptic digestion of AE-betaX (or betaX+betaA) chains; separation of peptides by fingerprinting or reversed phase HPLC; amino acid analysis; sequencing | |
DNA ANALYSES | |
A GTG->ATG mutation at codon 109 (Ref. 5) | |
FUNCTION STUDIES | |
Increased oxygen affinity; normal Bohr effect; decreased cooperativity | |
STABILITY | |
Normal | |
OCCURRENCE | |
Found in a Filipino family living in the USA, in an Anglo-Saxon family in England, in a Japanese family, and in a West Indian family | |
OTHER INFORMATION | |
Quantity in the heterozygotes not provided; occurred in combination with Hb S (Ref. 5) | |
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REFERENCES |
1. | |
Nute, P.E., Stamatoyannopoulos, G., Hermodson, M.A., and Roth, D.: J. Clin. Invest., 53:320, 1974. | |
2. | |
Anderson, N.L.: J. Clin. Invest., 53:329, 1974. | |
3. | |
Chanarin, I., Samson, D., Lang, A., Casey, R., Lorkin, P.A., and Lehmann, H.: Br. J. Haematol., 30:167, 1975. | |
4. | |
Nakatsuji, T., Wilson, J.B., Lam, H., and Huisman, T.H.J.: J. Chromatogr., 259: 511, 1983. | |
5. | |
Williamson, D., Perry, D.J., Brown, K., Langdown, J.V., and de Silva, C.: Hemoglobin, 19:27, 1995. | |