LRRK2 parkinsonism in Tunisia and Norway: a comparative analysis of disease penetrance
- PMID: 25008396
- PMCID: PMC4142000
- DOI: 10.1212/WNL.0000000000000675
LRRK2 parkinsonism in Tunisia and Norway: a comparative analysis of disease penetrance
Abstract
In recent years, the molecular etiology of parkinsonism has yielded to genetic analysis.1 Mutations in the gene leucine-rich repeat kinase 2 (LRRK2) have the highest genotypic and population attributable risk. Disparate penetrance estimates have been reported using a variety of statistical analyses, ethnic populations, and sample sizes.2 We compared the age-associated cumulative incidence (penetrance) of LRRK2 p.G2019S patients from Tunisia and Norway.
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