References
- King M. A.R., Wiltshire B. G., Lehmann H., Morimoto H. An unstable haemoglobin with reduced oxygen affinity: Haemoglobin Peterborough, β111 (G13) Valine→Phenylalanine, its interaction with normal haemoglobin and with Haemoglobin Lepore. Br. J. Haematol. 1972; 22: 125–134
- Nakanishi T., Miyazaki A., Kishikawa M., Shimizu A., Aoki Y., Kikuchi M. Hb Peterborough [β111(G13)Val→Phe] in Japan; rapid identification by ESI/MS using proteolytic digests of oxidized globin. Hemoglobin 1998; 22: 23–35
- Carrell R. W., Kay R. A simple method for the detection of unstable haemoglobins. Br. J. Haematol. 1972; 23: 615–619
- Marsh G., Marino G., Pucci P., Ferranti P., Malorni A., Kaeda J., Marsh J., Luzzato L. A third instance of the high oxygen affinity variant, Hb Heathrow [β103(G5) Phe→Leu]: identification of the mutation by mass spectrometry and by DNA analysis. Hemoglobin 1991; 15: 43–51
- Carbone V., Salzano A. M., Pagano L., Viola A., Buffardi S., De Rosa C., Pucci P. Hb Rainier [β145(HC2)Tyr→Cys] in Italy. Characterization of the amino acid substitution and the DNA mutation. Hemoglobin 1999; 23: 111–124
- Old J. M., Varawalla N. Y., Weatherall D. J. Rapid detection and prenatal diagnosis of α-thalassaemia: studies in Indian and Cypriot populations in the UK. The Lancet 1990; 6: 834–837
- Orkin S. H., Kazazian H. H., Jr., Antonarakis S. E., Goff S. C., Boehm C. D., Sexton J. P., Waber P. G., Giardina P. J.V. Linkage of β-thalassaemia mutations and β-globin gene polymorphisms with DNA polymorphisms in human β-globin gene cluster. Nature 1982; 296: 627–631
- Como P. F., Wylie B. R., Trent R. J., Bruce D., Volpato F., Wilkinson T., Kronenberg H., Holland R. A.B., Tibben E. A. A new unstable and low oxygen affinity hemoglobin variant: Hb Stanmore [β111(G13) Val→Ala]. Hemoglobin 1991; 15: 53–65