JSIMD Meeting
Putative genetic deficiency of 4-hydroxyphenylpyruvic acid dioxygenase in mice: A murine model for hereditary tyrosinaemia type III
F. Endo,
F. Endo
Department of Paediatrics, Kumamoto University Medical School, Honjo 1-1-1, Kumamoto, 860 Japan
Search for more papers by this author H. Katoh,
H. Katoh
Laboratory of Genetics, Central Institute for Experimental Animals, Kawasaki, 213 Japan
Search for more papers by this author I. Matsuda,
I. Matsuda
Department of Paediatrics, Kumamoto University Medical School, Honjo 1-1-1, Kumamoto, 860 Japan
Search for more papers by this author
F. Endo,
F. Endo
Department of Paediatrics, Kumamoto University Medical School, Honjo 1-1-1, Kumamoto, 860 Japan
Search for more papers by this author H. Katoh,
H. Katoh
Laboratory of Genetics, Central Institute for Experimental Animals, Kawasaki, 213 Japan
Search for more papers by this author I. Matsuda,
I. Matsuda
Department of Paediatrics, Kumamoto University Medical School, Honjo 1-1-1, Kumamoto, 860 Japan
Search for more papers by this author
First published: 01 September 1990
No abstract is available for this article.
References
- 1Berger R., Smit G.P., Stoker-de Vries S.A., Duran M., Ketting D., Wadman S.K. (1981) Deficiency of fumarylacetoacetase in a patient with hereditary tyrosinemia. Clin. Chim. Acta, 114: 37–44.
- 2Endo F., Kitano A., Uehara I., Nagata N., Matsuda I., Shinka T., Kuhara T., Matsumoto I. (1983) 4-Hydroxyphenylpyruvic acid oxidase deficiency with normal fumarylacetoacetase: a new variant form of hereditary hypertyrosinemia. Pediatr. Res., 17: 92–96.
- 3Fellman J.H., Fujita T.S., Roth E.S. (1972) Assay, properties and tissue distribution ofp-hydroxyphenylpyruvate hydroxylase. Biochim. Biophys. Acta, 284: 90–100.
- 4Giardini O., Cantani A., Kennaway N.G., D'Eufemia P. (1983) Chronic tyrosinemia associated with 4-hydroxyphenylpyruvic acid dioxygenase deficiency with acute intermittent ataxia and without visceral and bone involvement. Pediatr. Res., 17: 25–29.
- 5Kennaway N.G., Buist N.R.M. (1971) Metabolic studies in a patient with hepatic cytosol tyrosine aminotransferase deficiency. Pediatr. Res., 5: 287–297.
- 6Louis W.J., Pitt D.D., Davies H. (1974) Biochemical studies in a patient with ‘Tyrosinosis’. Aust. NZ J. Med., 4: 281–286.
