Molecular basis of phenylketonuria and its clinical applications

Mol Biol Med. 1987 Aug;4(4):183-92.
No abstract available

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.
  • Review

MeSH terms

  • Gene Frequency
  • Genetic Carrier Screening
  • Haplotypes
  • Humans
  • Mutation
  • Phenylalanine Hydroxylase / genetics*
  • Phenylketonurias / diagnosis
  • Phenylketonurias / physiopathology*
  • Polymorphism, Restriction Fragment Length

Substances

  • Phenylalanine Hydroxylase