Putative genetic deficiency of 4-hydroxyphenylpyruvic acid dioxygenase in mice: A murine model for hereditary tyrosinaemia type III
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://www.springerlink.com/index/pdf/10.1007/BF01799587
Reference6 articles.
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) 37–44
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) 92–96
3. Fellman, J.H., Fujita, T.S. and Roth, E.S. Assay, properties and tissue distribution ofp-hydroxyphenylpyruvate hydroxylase.Biochim. Biophys. Acta 284 (1972) 90–100
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) 25–29
5. Kennaway, N.G. and Buist, N.R.M. Metabolic studies in a patient with hepatic cytosol tyrosine aminotransferase deficiency.Pediatr. Res. 5 (1971) 287–297
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