FXTAS, SCA10, and SCA17 in American patients with movement disorders

Am J Med Genet A. 2005 Jul 1;136(1):87-9. doi: 10.1002/ajmg.a.30761.
No abstract available

Publication types

  • Letter
  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Adolescent
  • Adult
  • Aged
  • Aged, 80 and over
  • Ataxia / genetics
  • Ataxia / pathology*
  • Child
  • Child, Preschool
  • Female
  • Fragile X Mental Retardation Protein
  • Fragile X Syndrome / pathology*
  • Humans
  • Male
  • Microsatellite Repeats / genetics
  • Middle Aged
  • Movement Disorders / genetics
  • Movement Disorders / pathology*
  • Nerve Tissue Proteins / genetics
  • RNA-Binding Proteins / genetics
  • Spinocerebellar Ataxias / genetics
  • Spinocerebellar Ataxias / pathology*
  • TATA-Box Binding Protein / genetics
  • Tremor / genetics
  • Tremor / pathology*
  • Trinucleotide Repeat Expansion / genetics
  • United States

Substances

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