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Clinical and Pathological Characteristics ofLRRK2G2019S Patients with PD

✍ Scribed by Markos Poulopoulos; Etty Cortes; Jean-Paul G. Vonsattel; Stanley Fahn; Cheryl Waters; Lucien J. Cote; Carol Moskowitz; Lawrence S. Honig; Lorraine N. Clark; Karen S. Marder; Roy N. Alcalay


Book ID
113093554
Publisher
Humana Press Inc
Year
2011
Tongue
English
Weight
353 KB
Volume
47
Category
Article
ISSN
0895-8696

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## Abstract 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