Article
Familial Parkinsonism and early onset Parkinson's disease in a Brazilian movement disorders clinic: phenotypic characterization and frequency of SNCA, PRKN, PINK1, and LRRK2 mutations.
Movement disorders : official journal of the Movement Disorder Society - 15 Apr 2009
Camargos Sarah Teixeira, Dornas Leonardo Oliveira, Momeni Parastoo, Lees Andrew, Hardy John, Singleton Andrew, Cardoso Francisco
Abstract excerpt
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 sequencing...
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