Triplet repeat expansion mutations: the example of fragile X syndrome

Annu Rev Neurosci. 1995:18:77-99. doi: 10.1146/annurev.ne.18.030195.000453.
No abstract available

Publication types

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

MeSH terms

  • Female
  • Fragile X Syndrome / genetics*
  • Humans
  • Male
  • Methylation
  • Mutation
  • Oligonucleotides / genetics*
  • Pedigree
  • Repetitive Sequences, Nucleic Acid

Substances

  • Oligonucleotides