Trinucleotide repeat disorders

J Inherit Metab Dis. 1997 Jun;20(2):122-4. doi: 10.1023/a:1005388218625.
No abstract available

MeSH terms

  • Fragile X Syndrome / genetics
  • Humans
  • Huntington Disease / genetics
  • Metabolic Diseases / genetics*
  • Muscular Atrophy, Spinal / genetics
  • Myotonic Dystrophy / genetics
  • Trinucleotide Repeats*