Article
LRRK2 and Parkinson's disease in Norway.
Acta neurologica Scandinavica. Supplementum - 1 Jan 2007
Toft M, Haugarvoll K, Ross O A, Farrer M J, Aasly J O
Abstract excerpt
OBJECTIVES: Mutations in the LRRK2 gene have been associated with both familial and sporadic late-onset Parkinson's disease. A large number of mutations in this gene have been identified; however, for many of these variants, the pathogenicity and relative frequency are unknown. Herein, we investi...
Topics
- Adult
- Aged
- Aged, 80 and over
- Asian People
- DNA Mutational Analysis
- Female
- Gene Frequency
- Genetic Markers
- Genetic Predisposition to Disease
- Genetic Testing
- Genotype
- Humans
- Introns
- Leucine-Rich Repeat Serine-Threonine Protein Kinase-2
- Male
- Middle Aged
- Mutation
- Norway