The role of the alpha-synuclein gene mutation in patients with sporadic Parkinson's disease in the United Kingdom

J Neurol Neurosurg Psychiatry. 1998 Sep;65(3):378-9. doi: 10.1136/jnnp.65.3.378.

Abstract

Parkinson's disease is a common neurodegenerative disorder of unknown aetiology. A pathogenic point mutation within the a-synuclein gene has recently been identified in one Italian-American kindred and three families of Greek origin with parkinsonism. DNA from 70 patients with Parkinson's disease was screened for this G209A mutation. No samples were positive for the mutation, suggesting that it is not relevant for most patients with sporadic idiopathic Parkinson's disease.

MeSH terms

  • DNA Mutational Analysis
  • Genetic Testing
  • Humans
  • Nerve Tissue Proteins / genetics*
  • Parkinson Disease / diagnosis
  • Parkinson Disease / genetics*
  • Point Mutation / genetics*
  • Polymerase Chain Reaction
  • Synucleins
  • United Kingdom
  • alpha-Synuclein

Substances

  • Nerve Tissue Proteins
  • SNCA protein, human
  • Synucleins
  • alpha-Synuclein