Multiple founder effects in Japanese families with primary torsion dystonia harboring the GAG deletion in the Tor1A (DYT1) gene

Neurogenetics. 2002 Oct;4(2):105-6. doi: 10.1007/s10048-002-0135-7.
No abstract available

Publication types

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

MeSH terms

  • Carrier Proteins / genetics*
  • Dystonia Musculorum Deformans / genetics*
  • Family Health
  • Female
  • Founder Effect*
  • Gene Deletion*
  • Haplotypes
  • Humans
  • Japan
  • Male
  • Molecular Chaperones*

Substances

  • Carrier Proteins
  • Molecular Chaperones
  • TOR1A protein, human