Identification of a Novel LRRK2 Mutation Linked to Autosomal Dominant Parkinsonism: Evidence of a Common Founder across European Populations
- 1 April 2005
- journal article
- Published by Elsevier BV in American Journal of Human Genetics
- Vol. 76 (4), 672-680
- https://doi.org/10.1086/429256
Abstract
No abstract availableKeywords
This publication has 37 references indexed in Scilit:
- Cloning of the Gene Containing Mutations that Cause PARK8-Linked Parkinson's DiseaseNeuron, 2004
- α-synuclein locus duplication as a cause of familial Parkinson's diseaseThe Lancet, 2004
- Parkin genetics: one model for Parkinson's diseaseHuman Molecular Genetics, 2004
- The new mutation, E46K, of α‐synuclein causes parkinson and Lewy body dementiaAnnals of Neurology, 2003
- α-Synuclein Locus Triplication Causes Parkinson's DiseaseScience, 2003
- Mutations of the BRAF gene in human cancerNature, 2002
- AlaSOPro mutation in the gene encoding α-synuclein in Parkinson's diseaseNature Genetics, 1998
- Mutation in the α-Synuclein Gene Identified in Families with Parkinson's DiseaseScience, 1997
- Prevalence of Parkinson's disease in the elderlyNeurology, 1995
- Genetic dissection of complex traits: guidelines for interpreting and reporting linkage resultsNature Genetics, 1995