Expanding the phenotype of fragile X-associated tremor/ataxia syndrome: a new female case

Mov Disord. 2007 Aug 15;22(11):1677-8. doi: 10.1002/mds.21571.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Aged
  • Ataxia / etiology*
  • Ataxia / genetics
  • Ataxia / pathology
  • Female
  • Fragile X Mental Retardation Protein / genetics
  • Fragile X Syndrome / complications*
  • Fragile X Syndrome / genetics
  • Humans
  • Magnetic Resonance Imaging
  • Mutation / genetics
  • Phenotype*
  • Tremor / etiology*
  • Tremor / genetics
  • Tremor / pathology

Substances

  • FMR1 protein, human
  • Fragile X Mental Retardation Protein