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Clinical, neuropathological and genotypic variability in SNCA A53T familial Parkinson’s disease

✍ Scribed by K. Markopoulou; D. W. Dickson; R. D. McComb; Z. K. Wszolek; L. Katechalidou; L. Avery; M. S. Stansbury; B. A. Chase

Book ID
106073660
Publisher
Springer-Verlag
Year
2008
Tongue
English
Weight
739 KB
Volume
116
Category
Article
ISSN
0001-6322

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## Abstract The aim of the study was to evaluate the frequency and to perform phenotypic and genotypic characterization of familial Parkinsonism and early onset Parkinson's disease (EOPD) in a Brazilian movement disorder unit. We performed a standardized clinical assessment of patients followed by