Journal of Inherited Metabolic Disease

, Volume 13, Issue 5, pp 780–782 | Cite as

Putative genetic deficiency of 4-hydroxyphenylpyruvic acid dioxygenase in mice: A murine model for hereditary tyrosinaemia type III

  • F. Endo
  • H. Katoh
  • I. Matsuda
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Keywords

Public Health Internal Medicine Metabolic Disease Murine Model Genetic Deficiency 

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References

  1. Berger, R., Smit, G.P., Stoker-de Vries, S.A., Duran, M., Ketting, D. and Wadman, S.K. Deficiency of fumarylacetoacetase in a patient with hereditary tyrosinemia.Clin. Chim. Acta 114 (1981) 37–44Google Scholar
  2. Endo, F., Kitano, A., Uehara, I., Nagata, N., Matsuda, I., Shinka, T., Kuhara, T. and Matsumoto, I. 4-Hydroxyphenylpyruvic acid oxidase deficiency with normal fumarylacetoacetase: a new variant form of hereditary hypertyrosinemia.Pediatr. Res. 17 (1983) 92–96Google Scholar
  3. Fellman, J.H., Fujita, T.S. and Roth, E.S. Assay, properties and tissue distribution ofp-hydroxyphenylpyruvate hydroxylase.Biochim. Biophys. Acta 284 (1972) 90–100Google Scholar
  4. Giardini, O., Cantani, A., Kennaway, N.G. and D'Eufemia, P. Chronic tyrosinemia associated with 4-hydroxyphenylpyruvic acid dioxygenase deficiency with acute intermittent ataxia and without visceral and bone involvement.Pediatr. Res. 17 (1983) 25–29Google Scholar
  5. Kennaway, N.G. and Buist, N.R.M. Metabolic studies in a patient with hepatic cytosol tyrosine aminotransferase deficiency.Pediatr. Res. 5 (1971) 287–297Google Scholar
  6. Louis, W.J., Pitt, D.D. and Davies, H. Biochemical studies in a patient with ‘Tyrosinosis’.Aust. NZ J. Med. 4 (1974) 281–286Google Scholar

Copyright information

© SSIEM and Kluwer Academic Publishers 1990

Authors and Affiliations

  • F. Endo
    • 1
  • H. Katoh
    • 2
  • I. Matsuda
    • 1
  1. 1.Department of PaediatricsKumamoto University Medical SchoolKumamotoJapan
  2. 2.Laboratory of GeneticsCentral Institute for Experimental AnimalsKawasakiJapan

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