Lack of association with TorsinA haplotype in German patients with sporadic dystonia

Neurology. 2006 Mar 28;66(6):951-2. doi: 10.1212/01.wnl.0000203344.43342.18.
No abstract available

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Alleles
  • Dystonic Disorders / genetics*
  • Female
  • Genetic Linkage / genetics
  • Germany
  • Haplotypes / genetics*
  • Humans
  • Male
  • Middle Aged
  • Molecular Chaperones / genetics*

Substances

  • Molecular Chaperones
  • TOR1A protein, human