Novel LRRK2 mutation in the Roc domain in an Western Australian family with autosomal dominant late-onset Parkinson's disease (LOPD)

F. L. Mastaglia, Y. Huang, G. Halliday, D. B. Rowe, C. M. Sue

    Research output: Contribution to journalMeeting abstract

    Original languageEnglish
    Pages (from-to)729-729
    Number of pages1
    JournalMovement Disorders
    Issue numberSuppl. 16
    Publication statusPublished - 2007

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