The p.S77N presenilin-associated rhomboid-like protein mutation is not a frequent cause of early-onset Parkinson's disease

Mov Disord. 2011 Nov;26(13):2441-2. doi: 10.1002/mds.23889. Epub 2011 Sep 23.
No abstract available

Publication types

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

MeSH terms

  • Age of Onset
  • Genetic Variation
  • Humans
  • Metalloproteases / genetics*
  • Mitochondrial Proteins / genetics*
  • Mutation / genetics
  • Parkinson Disease / genetics*

Substances

  • Mitochondrial Proteins
  • Metalloproteases
  • PARL protein, human