A novel point mutation in the GTP cyclohydrolase I gene in a Spanish family with hereditary progressive and dopa responsive dystonia

J Neurol Neurosurg Psychiatry. 1997 Apr;62(4):420-1. doi: 10.1136/jnnp.62.4.420.
No abstract available

Publication types

  • Clinical Trial
  • Controlled Clinical Trial
  • Letter

MeSH terms

  • Dystonia / genetics*
  • GTP Cyclohydrolase / genetics*
  • Humans
  • Nucleotide Mapping
  • Pedigree
  • Point Mutation*

Substances

  • GTP Cyclohydrolase