REFERENCES
- Nathan DG, Oski FA, Eds. Nathan and Oski’s Hematology of Infancy and Childhood, 6th ed. Philadelphia: W.B. Saunders. 2003.
- Hb Var: a database of human hemoglobin variants and thalassemias (http://globin.cse. psu.edu/hbvar/menu/html).
- Babb A, Solaiman S, Green BN, Mantio D, Patel K. Hb Hillingdon [α46(CE4)Phe→Val (α1 or α2)]: a new α chain hemoglobin variant. Hemoglobin. 2009;33(6):503–506.
- Ng PC, Henikoff S. Predicting deleterious amino acid substitutions. Genome Res. 2001;11(5):863–874.
- Ramensky V, Bork P, Sunyaev S. Human non-synonymous SNPs: server and survey. Nucleic Acids Res. 2002;30(17):3894–3900.
- Perutz MF. Mechanisms of cooperativity and allosteric regulation in proteins. Q Rev Biophys.1989;22(2):139–237.
- Yang F, Phillips GN, Jr. Crystal structures of CO-, deoxy- and met-myoglobins at various pH values. J Mol Biol. 1996;256(4):762–774.