1. G.A. Mitchell, M. Lambert, R.M. Tanguary. in: C.R. Scriver, A.L. Beaudet, W.S. Sly, D. Valle (Eds.), The Metabolic and Molecular Bases of Inherited Disease, seventh ed., McGraw-Hill, New York, 1995, p. 1077.
2. E.A. Kvittingen, E. Holme, in: J. Fernandes, J.-M. Saudubray, G. van den Berghe (Eds.), Inborn Metabolic Diseases, third ed., Springer, Berlin, 2000, p. 187.
3. On the enzymic defects in hereditary tyrosinemia.
4. Dietary treatment eliminates succinylacetone from the urine of a patient with tyrosinaemia type 1
5. Tyrosinaemia type I — an update