Phenotypic variability in a large kindred (Family LA) with deletions in the parkin gene

Mov Disord. 2002 Mar;17(2):424-6. doi: 10.1002/mds.10071.
No abstract available

Publication types

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

MeSH terms

  • Adult
  • Aged
  • Aged, 80 and over
  • Chromosome Deletion*
  • Female
  • Humans
  • Ligases / genetics*
  • Male
  • Middle Aged
  • Neurologic Examination
  • Parkinson Disease / diagnosis
  • Parkinson Disease / genetics*
  • Pedigree
  • Phenotype*
  • Ubiquitin-Protein Ligases*

Substances

  • Ubiquitin-Protein Ligases
  • parkin protein
  • Ligases