The enzyme defects in hereditary tyrosinaemia type I

J Inherit Metab Dis. 1984:7 Suppl 2:137-8. doi: 10.1007/978-94-009-5612-4_43.
No abstract available

MeSH terms

  • Amino Acid Metabolism, Inborn Errors / enzymology*
  • Humans
  • Hydrolases / deficiency*
  • Infant, Newborn
  • Kidney / enzymology
  • Liver / enzymology
  • Phenylpyruvic Acids / metabolism
  • Tyrosine / blood*

Substances

  • Phenylpyruvic Acids
  • 4-hydroxyphenylpyruvic acid
  • Tyrosine
  • Hydrolases
  • fumarylacetoacetase