Article
The biology and pathobiology of LRRK2: implications for Parkinson's disease.
Parkinsonism & related disorders - 1 Jan 2008
Moore Darren J
Abstract excerpt
Mutations in the leucine-rich repeat kinase 2 (LRRK2) gene are an important cause of late-onset, familial and sporadic Parkinson's disease. LRRK2 is a large unique protein containing both GTPase and kinase enzymatic domains together with multiple protein-protein interaction domains. LRRK2 initial...
Topics
- Animals
- Biology
- GTP Phosphohydrolases
- Genetic Predisposition to Disease
- Humans
- Inclusion Bodies
- Leucine-Rich Repeat Serine-Threonine Protein Kinase-2
- Mutation
- Parkinson Disease
- Protein Serine-Threonine Kinases
