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- W1969094603 abstract "Journal of Inherited Metabolic DiseaseVolume 13, Issue 5 p. 780-782 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 JapanSearch for more papers by this authorH. Katoh, H. Katoh Laboratory of Genetics, Central Institute for Experimental Animals, Kawasaki, 213 JapanSearch for more papers by this authorI. Matsuda, I. Matsuda Department of Paediatrics, Kumamoto University Medical School, Honjo 1-1-1, Kumamoto, 860 JapanSearch for more papers by this author F. Endo, F. Endo Department of Paediatrics, Kumamoto University Medical School, Honjo 1-1-1, Kumamoto, 860 JapanSearch for more papers by this authorH. Katoh, H. Katoh Laboratory of Genetics, Central Institute for Experimental Animals, Kawasaki, 213 JapanSearch for more papers by this authorI. Matsuda, I. Matsuda Department of Paediatrics, Kumamoto University Medical School, Honjo 1-1-1, Kumamoto, 860 JapanSearch for more papers by this author First published: 01 September 1990 https://doi.org/10.1007/BF01799587Citations: 4AboutPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL Share a linkShare onEmailFacebookTwitterLinkedInRedditWechat 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. Citing Literature Volume13, Issue5September 1990Pages 780-782 ReferencesRelatedInformation" @default.
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- W1969094603 title "Putative genetic deficiency of 4‐hydroxyphenylpyruvic acid dioxygenase in mice: A murine model for hereditary tyrosinaemia type III" @default.
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