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CONTACT | |
Internal | |
HEMATOLOGY | |
Heinz body hemolytic anemia in the heterozygote | |
ELECTROPHORESIS | |
Hb X and Hb A separate at alkaline pH; Hb X moves like Hb J | |
CHROMATOGRAPHY | |
Hb X was isolated by DEAE-Sephadex chromatography | |
STRUCTURE STUDIES | |
Tryptic digestion; separation of peptides by fingerprinting; amino acid analysis; thermolysin | |
DNA ANALYSES | |
Not reported; presumed mutation GGC->GAC at codon 74 | |
FUNCTION STUDIES | |
Increased oxygen affinity; decreased 2,3-DPG effect | |
STABILITY | |
Unstable | |
OCCURRENCE | |
Found in a South African female of British origin; a father and three daughters of one Sicilian family, and two siblings of another Sicilian family | |
OTHER INFORMATION | |
Quantity in the heterozygote about 24% | |
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REFERENCES |
1. | |
White, J.M., Brain, M.C., Lorkin, P.A., Lehmann, H., and Smith, M.: Nature, 225: 939, 1970. | |
2. | |
May, A. and Huehns, E.R.: Br. J. Haematol., 22:599, 1972. | |
3. | |
Sansone, G., Sciarratta, G.V., Genova, R., Darbre, P.D., and Lehmann, H.: Acta Haematol., 57:102, 1977. | |
4. | |
Schiliro, G., Musumeci, S., Russo, A., Russo, G., Marinucci, M., Giampaola, A., Cianetti, L., and Tentori, L.: Hemoglobin, 5:493, 1981. | |