## 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
✦ LIBER ✦
Identification of the novel D297fsX318 PINK1 mutation and phenotype variation in a family with early-onset Parkinson's disease
✍ Scribed by Giovanni Savettieri; Grazia Annesi; Donatella Civitelli; Innocenza Claudia Cirò Candiano; Giuseppe Salemi; Paolo Ragonese; Ferdinanda Annesi; Patrizia Tarantino; Valeria Terruso; Marco D'Amelio; Aldo Quattrone
- Book ID
- 116820427
- Publisher
- Elsevier Science
- Year
- 2008
- Tongue
- English
- Weight
- 470 KB
- Volume
- 14
- Category
- Article
- ISSN
- 1353-8020
No coin nor oath required. For personal study only.
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