A specific mutation for Huntington's disease

J Med Genet. 1993 Dec;30(12):975-7. doi: 10.1136/jmg.30.12.975.
No abstract available

Publication types

  • Editorial
  • Review

MeSH terms

  • Female
  • Humans
  • Huntington Disease / diagnosis
  • Huntington Disease / genetics*
  • Male
  • Mutation
  • Oligodeoxyribonucleotides / genetics
  • Repetitive Sequences, Nucleic Acid

Substances

  • Oligodeoxyribonucleotides