The origin of urinary p-hydroxyphenylpyruvate in a patient with hepatic cytosol tyrosine aminotransferase deficiency
- 31 October 1972
- journal article
- Published by Elsevier in Clinica Chimica Acta; International Journal of Clinical Chemistry
- Vol. 41, 157-161
- https://doi.org/10.1016/0009-8981(72)90506-2
Abstract
No abstract availableKeywords
This publication has 5 references indexed in Scilit:
- Metabolic Studies in a Patient with Hepatic Cytosol Tyrosine Aminotransferase DeficiencyPediatric Research, 1971
- Soluble and mitochondrial forms of tyrosine aminotransferase. Relation to human tyrosinemiaBiochemistry, 1969
- Crystalline oxidase from the soluble fraction of rat kidney cellsBiochimica et Biophysica Acta (BBA) - Enzymology, 1967
- The renal clearance of phenylpyruvateClinica Chimica Acta; International Journal of Clinical Chemistry, 1961
- The Determination of Endogenous Creatinine in Plasma and UrineScandinavian Journal of Clinical and Laboratory Investigation, 1953