A new variant form of hypertyrosinaemia due to 4‐hydroxyphenylpyruvic acid oxidase deficiency
- 1 December 1982
- journal article
- case report
- Published by Wiley in Journal of Inherited Metabolic Disease
- Vol. 5 (4) , 237-238
- https://doi.org/10.1007/bf02179153
Abstract
No abstract availableKeywords
This publication has 7 references indexed in Scilit:
- Deficiency of fumarylacetoacetase in a patient with hereditary tyrosinemiaClinica Chimica Acta; International Journal of Clinical Chemistry, 1981
- Hereditary tyrosinemia - fumarylacetoacetase deficiencyPediatric Research, 1979
- On the enzymic defects in hereditary tyrosinemia.Proceedings of the National Academy of Sciences, 1977
- Radiochemical assays for p-hydroxyphenylpyruvate hydroxylase activity in human liverClinica Chimica Acta; International Journal of Clinical Chemistry, 1971
- Metabolic Studies in a Patient with Hepatic Cytosol Tyrosine Aminotransferase DeficiencyPediatric Research, 1971
- Assay of tyrosine transaminase activity by conversion of p-hydroxyphenylpyruvate to p-hydroxybenzaldehydeAnalytical Biochemistry, 1966
- THE ENZYMATIC CONVERSION OF HOMOGENTISIC ACID TO 4-FUMARYLACETOACETIC ACIDJournal of Biological Chemistry, 1951