Point mutations in exon 1 of the NR4A2 gene are not a major cause of familial Parkinson's disease [1]

Alexander Zimprich, Friedrich Asmus, Petra Leitner, Mirna Castro, Benjamin Bereznai, Nikolaus Homann, Erwin Ott, A. Wijnand, F. Rutgers, Gyri Wieditz, Claudia Trenkwalder, Thomas Gasser

Research output: Contribution to journalLetter

25 Citations (Scopus)
Original languageEnglish
Pages (from-to)219-220
Number of pages2
JournalNeurogenetics
Volume4
Issue number4
DOIs
Publication statusPublished - Aug 1 2003

Keywords

  • Familial Parkinson's disease
  • NR4A2 gene
  • Point mutations

ASJC Scopus subject areas

  • Genetics
  • Genetics(clinical)
  • Cellular and Molecular Neuroscience

Cite this

Zimprich, A., Asmus, F., Leitner, P., Castro, M., Bereznai, B., Homann, N., Ott, E., Wijnand, A., Rutgers, F., Wieditz, G., Trenkwalder, C., & Gasser, T. (2003). Point mutations in exon 1 of the NR4A2 gene are not a major cause of familial Parkinson's disease [1]. Neurogenetics, 4(4), 219-220. https://doi.org/10.1007/s10048-003-0156-x