Point mutation in intron 10 of FMR1 is unlikely to be a cause of fragile X syndrome

Hum Mutat. 1998;12(6):431-2. doi: 10.1002/(SICI)1098-1004(1998)12:6<431::AID-HUMU10>3.0.CO;2-Y.
No abstract available

Publication types

  • Comment
  • Letter

MeSH terms

  • Fragile X Mental Retardation Protein
  • Fragile X Syndrome / genetics*
  • Humans
  • Introns / genetics*
  • Male
  • Nerve Tissue Proteins / genetics*
  • Point Mutation / genetics*
  • RNA-Binding Proteins*

Substances

  • FMR1 protein, human
  • Nerve Tissue Proteins
  • RNA-Binding Proteins
  • Fragile X Mental Retardation Protein