Mutations and mechanism: how PINK1 may contribute to risk of sporadic Parkinson's disease

Brain. 2017 Jan;140(1):2-5. doi: 10.1093/brain/aww320.
No abstract available

Publication types

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

MeSH terms

  • Heterozygote*
  • Humans
  • Mutation
  • Parkinson Disease*
  • Protein Kinases / genetics
  • Risk
  • Ubiquitin-Protein Ligases / genetics

Substances

  • Ubiquitin-Protein Ligases
  • Protein Kinases