1. Mitchell, G.A., Lambert, M. & Tanguay, P.M. in The metabolic and molecular basis of inherited disease, (eds Scriver, C.R., Beaudet, A.L, Sly, W. & Valte, D.) 1077–1106 (MacGraw-Hill, New York, 1994).
2. Russo, P. & O'Regan, S. Visceral pathology of hereditary tyrosinemia type I. Am. J. hum. Genet. 47, 317–324 (1990).
3. Mitchell, G. et al Neurologic crises in hereditary tyrosinemia. New Engl. J. Med. 322, 432–437 (1990).
4. Perry, T.L. Tyrosinemia associated with hypermethioninemia and islet cell hyperplasia. Can. Med. Ass. J. 97, 1067–1075 (1967).
5. Edwards, M.A., Green, A., Colli, A. & Rylance, G. Tyrosinaemia type I and hypertrophic obstructive cardiomyopathy. Lancet. 1, 1437–1438 (1987).