REFERENCES
- Bayoumi RA, Dawodu A, Qureshi MM, The association of Hb Khartoum [β124(H2)Pro→Arg] with γ+-thalassemia is responsible for hemolytic disease in the newborn of a Sudanese family. Hemoglobin. 1999;23(1):33–45.
- Nakatsuji T, Shimizu K, Huisman THJ. Hb F-La Grange or α2γ2101(G3)Glu→Lys; 75Ile; 136Gly: a high oxygen affinity fetal hemoglobin variant observed in a Caucasian newborn. Biochim Biophys Acta. 1984;789(2):224–228.
- Adams JG3rd, Winter WP, Tausk K, Heller P. Hemoglobin Rush [β101 (G3) glutamine]: a new unstable hemoglobin causing mild hemolytic anemia. Blood. 1974;43(2):261–269.
- Shih DT, Jones RT, Imai K, Tyuma I. Involvement of Glu G3(101)β in the function of hemoglobin. Comparative O2 equilibrium studies of human mutant hemoglobins. J Biol Chem. 1985;260(10):5919–5924.