Genetic and clinical identification of Parkinson's disease patients with LRRK2 G2019S mutation
- 31 May 2005
- journal article
- letter
- Published by Wiley in Annals of Neurology
- Vol. 57 (6) , 933-934
- https://doi.org/10.1002/ana.20510
Abstract
No abstract availableKeywords
This publication has 5 references indexed in Scilit:
- Clinical and positron emission tomography of Parkinson's disease caused by LRRK2Annals of Neurology, 2005
- Cloning of the Gene Containing Mutations that Cause PARK8-Linked Parkinson's DiseaseNeuron, 2004
- Protein Kinases Linked to the Pathogenesis of Parkinson's DiseaseNeuron, 2004
- Hereditary Early-Onset Parkinson's Disease Caused by Mutations in PINK1Science, 2004
- Diagnostic Criteria for Parkinson DiseaseArchives of Neurology, 1999