α-Synuclein (SNCA) A30G Mutation as a Cause of a Complex Phenotype Without Parkinsonism

Mov Disord. 2021 Sep;36(9):2209-2212. doi: 10.1002/mds.28735.
No abstract available

Publication types

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

MeSH terms

  • Humans
  • Mutation / genetics
  • Parkinsonian Disorders* / diagnostic imaging
  • Parkinsonian Disorders* / genetics
  • Phenotype
  • alpha-Synuclein* / genetics

Substances

  • SNCA protein, human
  • alpha-Synuclein