Serum prolactin in symptomatic and asymptomatic dopa-responsive dystonia due to a GCH1 mutation

Neurology. 2003 Jul 22;61(2):269-70. doi: 10.1212/01.wnl.0000073983.82532.49.
No abstract available

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Substitution
  • Dihydroxyphenylalanine / therapeutic use*
  • Dystonic Disorders / blood
  • Dystonic Disorders / drug therapy
  • Dystonic Disorders / genetics*
  • Exons / genetics
  • Female
  • GTP Cyclohydrolase / deficiency
  • GTP Cyclohydrolase / genetics*
  • Genes, Dominant
  • Heterozygote
  • Humans
  • Male
  • Mutation, Missense*
  • Pedigree
  • Point Mutation*
  • Prolactin / blood*

Substances

  • Dihydroxyphenylalanine
  • Prolactin
  • GTP Cyclohydrolase