References
- Metha, A., Mason, P.J. and Vulliamy, T.J. (2000) "Glucose-6-phosphate dehydrogenase deficiency", Ballieres Clinical Haematology 13, 21–38.
- Fiorelli, G., Montemuros, M. and Cappellini, M. (2000) "Chronic non-spherocytic haemolytic disorders associated with glucose-6-phosphate dehydrogenase variants", Bailliere's Best Practice and Research 13, 39–55.
- Working WHO Group(1989) "Glucose-6-phosphate dehydro-genase deficiency", Bulletin of the World Health Organization 67, 601–611.
- Beutler, E., Claramma, K. and Joseph, S. (1968) "Biochemical variants of glucose-6-phosphate dehydrogenase giving rise to congenital non-spherocytic hemolytic disease", Blood 31, 131–144.
- Gordon-Smith, E. and White, J. (1974) "Oxidative haemolysis and heinz body haemolytic anaemia", British Journal of Haematology 26, 513–517.
- Mason, P., Sonati, M., Macdonald, D., Lanza, C., Busutil, D., Town, M., Corcoran, C.M., Kaeda, J.S., Stevens, D., Al-Ismail, S., Altay, C., Hatton, C., Lewis, D.S., McMullin, ME, Meloni, T., Paul, B., Pippard, M., Prentice, A.G., Vulliamy, T.J. and Luzzatto, L. (1995) "New glucose 6 phosphate dehydrogenase mutations associated with chronic anemia", Blood 85, 1377–1380.
- Vacca, C., Ibarra, B., Romero, F., Olivares, N., Cantu, J.M. and Beutler, E. (1982) "G-6-PD Guadalahaja. A new mutant associated with non-spherocytic haemolytic anaemia", Human Genetics 61, 175–176.
- Synder, L., Necheles, T. and Reddy, W. (1970) "G6PD Worchester: a new variant, associated with X-linked optic atrophy", American Journal of Medicine 49, 125–132.
- Rattazzi, M.C., Corash, L.M., Van Zanen, G.E., Jaffe, E.R. and Piomelli, S. (1971) "G6PD deficiency and chronic hemolysis: four new mutants—relationships between clinical syndrome and enzyme kinetics", Blood 38, 205–218.
- Vulliamy, T., Kaeda, J.S., Ait-Chafa, D., et al. (1998) "Clinical and hamatological consequences of recurrent G6PD mutations and a new mutation causing chronic non spherocytic haemolytic anaemia", British Journal of Haemato-logy 101, 670–675.
- Forni, G., Napoli, G., Gaetani, G. and Ferraris, A. (1994) "G6PD deficiency related chronic hemolysis treated with splenectomy: a case report", American Journal of Haematology 47(2), 146–147.
- Ravindraneth, Y. and Beutler, E. (1987) "Two new variants of glucose 6 phosphate dehydrogenase associated with non-spherocytic hemolytic anaemia: G6PD wayne and huron", American Journal of Hematology 24, 357–363.
- Vives-Corrons, J.L., Assumpcio Pujades, M., Petit, J., Colomer, Corbella, M., Aguilar, I., Bascompte, J.L. and Merino, A. (1989) "Chronic nonspherocytic hemolytic anaemia (CNSHA) and glucose-6-phosphate dehydrogenase (G6PD) in a patient with familial amyloidotic polyneuro-pathy (FAP)", Human Genetics 81, 161–164.
- Luzzatto, L. (1975) "Inherited haemolytic states: Glucose-6-Phosphate dehydrogenase deficiency", Clinics in Haematology 4(1), 83–108.
- Luzzatto, L. (1996) "Glucose-6-phosphate dehydrogenase (G6PD) deficiency", Oxford Textbook of Medicine, 3537–3541.