DJ-1 mutations are a rare cause of recessively inherited early onset parkinsonism mediated by loss of protein function.

P. J. Lockhart, S. Lincoln, M. Hulihan, J. Kachergus, K. Wilkes, G. Bisceglio, D. C. Mash, M. J. Farrer

Research output: Contribution to journalLetter

65 Scopus citations
Original languageEnglish (US)
Pages (from-to)e22
JournalJournal of medical genetics
Volume41
Issue number3
DOIs
StatePublished - Mar 2004

ASJC Scopus subject areas

  • Genetics
  • Genetics(clinical)

Cite this

Lockhart, P. J., Lincoln, S., Hulihan, M., Kachergus, J., Wilkes, K., Bisceglio, G., Mash, D. C., & Farrer, M. J. (2004). DJ-1 mutations are a rare cause of recessively inherited early onset parkinsonism mediated by loss of protein function. Journal of medical genetics, 41(3), e22. https://doi.org/10.1136/jmg.2003.011106