Absence of NR4A2 exon 1 mutations in 108 families with autosomal dominant Parkinson disease

Neurology. 2004 Jun 8;62(11):2133-4. doi: 10.1212/01.wnl.0000127496.23198.75.
No abstract available

Publication types

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

MeSH terms

  • Adult
  • Age of Onset
  • Aged
  • Aged, 80 and over
  • DNA Mutational Analysis
  • DNA-Binding Proteins / genetics*
  • Europe / ethnology
  • Exons / genetics
  • Female
  • France / epidemiology
  • Genes, Dominant
  • Humans
  • Male
  • Middle Aged
  • Nuclear Receptor Subfamily 4, Group A, Member 2
  • Parkinson Disease / epidemiology
  • Parkinson Disease / genetics*
  • Transcription Factors / genetics*

Substances

  • DNA-Binding Proteins
  • NR4A2 protein, human
  • Nuclear Receptor Subfamily 4, Group A, Member 2
  • Transcription Factors