The implications of multiple forms of phenylalanine hydroxylase in phenylketonuria and related diseases of phenylalanine metabolism

Biochem Med. 1976 Feb;15(1):55-86. doi: 10.1016/0006-2944(76)90074-0.
No abstract available

Publication types

  • Review

MeSH terms

  • Aging
  • Amino Acid Metabolism, Inborn Errors / enzymology*
  • Amino Acid Metabolism, Inborn Errors / genetics
  • Animals
  • Animals, Newborn
  • Female
  • Fetus
  • Genetic Variation
  • Gestational Age
  • Humans
  • Isoenzymes / metabolism*
  • Kinetics
  • Liver / enzymology
  • Liver / growth & development
  • Phenylalanine Hydroxylase / metabolism*
  • Phenylketonurias / enzymology*
  • Phenylketonurias / genetics
  • Phosphatidylcholines / pharmacology
  • Pregnancy
  • Rats

Substances

  • Isoenzymes
  • Phosphatidylcholines
  • Phenylalanine Hydroxylase