[Triplet repeat expansions in hereditary neurodegenerative diseases]

Med Clin (Barc). 1997 Apr 12;108(14):542-8.
[Article in Spanish]
No abstract available

Publication types

  • Review

MeSH terms

  • Adult
  • Ataxia / genetics
  • DNA / genetics*
  • Female
  • Fragile X Syndrome / genetics
  • Humans
  • Huntington Disease / genetics
  • Infant, Newborn
  • Male
  • Muscular Atrophy, Spinal / genetics
  • Mutation
  • Myotonic Dystrophy / genetics
  • Nervous System Diseases / genetics*
  • Trinucleotide Repeats*

Substances

  • DNA