Clinical and pathological characteristics of patients with Leucine-rich repeat kinase-2 mutations

Mutations in LRRK2 are the single most common known cause of Parkinson's disease (PD). Two new PD patients with LRRK2 mutation were identified from a cohort with extensive postmortem assessment. One of these patients harbors the R793M mutation and presented with the typical clinical and patholo...

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Veröffentlicht in:Movement disorders 2009-01, Vol.24 (1), p.32-39
Hauptverfasser: Covy, Jason P., Yuan, Wuxing, Waxman, Elisa A., Hurtig, Howard I., Van Deerlin, Vivianna M., Giasson, Benoit I.
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Sprache:eng
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