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 |
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Sprache: | eng |
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