Article
Is inhibition of kinase activity the only therapeutic strategy for LRRK2-associated Parkinson's disease?
BMC medicine - 23 Feb 2012
Rudenko Iakov N, Chia Ruth, Cookson Mark R
Abstract excerpt
Mutations in the leucine-rich repeat kinase 2 (LRRK2) gene are a common cause of familial Parkinson's disease (PD). Variation around the LRRK2 locus also contributes to the risk of sporadic PD. The LRRK2 protein contains a central catalytic region, and pathogenic mutations cluster in the Ras of c...
Topics
- Animals
- Clinical Trials as Topic
- Humans
- Mutation
- Parkinson Disease
- Protein Kinase Inhibitors
- Protein Serine-Threonine Kinases
- Translational Research, Biomedical
