The Ala53Thr mutation in the alpha-synuclein gene in a Korean family with Parkinson disease

Clin Genet. 2007 May;71(5):471-3. doi: 10.1111/j.1399-0004.2007.00781.x.
No abstract available

Publication types

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

MeSH terms

  • Adult
  • Age of Onset
  • Alanine / genetics
  • Amino Acid Substitution*
  • Family
  • Haplotypes
  • Humans
  • Korea
  • Male
  • Mutation
  • Parkinson Disease / genetics*
  • Parkinson Disease / pathology
  • Pedigree
  • Threonine / genetics
  • alpha-Synuclein / genetics*

Substances

  • alpha-Synuclein
  • Threonine
  • Alanine