Comparing LRRK2 Gly2385Arg carriers with noncarriers
- 15 April 2007
- journal article
- Published by Wiley in Movement Disorders
- Vol. 22 (5) , 749-750
- https://doi.org/10.1002/mds.21381
Abstract
No abstract availableThis publication has 4 references indexed in Scilit:
- Genetic Testing in Parkinson DiseaseArchives of Neurology, 2006
- A common missense variant in the LRRK2 gene, Gly2385Arg, associated with Parkinson’s disease risk in Taiwanneurogenetics, 2006
- Analysis of LRRK2 functional domains in nondominant Parkinson diseaseNeurology, 2005
- Mutations in LRRK2 Cause Autosomal-Dominant Parkinsonism with Pleomorphic PathologyNeuron, 2004