TY  - GEN
AU  - Ross,Owen A
AU  - Toft,Mathias
AU  - Haugarvoll,Kristoffer
TI  - Corticobasal syndrome and primary progressive aphasia as manifestations of lrrk2 gene mutations
SN  - 1526-632X
PY  - 2008///0902
KW  - Aphasia, Primary Progressive
KW  - genetics
KW  - Causality
KW  - DNA Mutational Analysis
KW  - standards
KW  - Genetic Markers
KW  - Genetic Predisposition to Disease
KW  - Genetic Testing
KW  - Genetic Variation
KW  - Genotype
KW  - Humans
KW  - Inheritance Patterns
KW  - Leucine-Rich Repeat Serine-Threonine Protein Kinase-2
KW  - Mutation
KW  - Neurodegenerative Diseases
KW  - Norway
KW  - Parkinson Disease
KW  - Protein Serine-Threonine Kinases
KW  - Risk Factors
N1  - Publication Type: Letter; Comment
UR  - https://doi.org/10.1212/01.wnl.0000320511.30222.dd
ER  -