Mutations in LRRK2 Cause Autosomal-Dominant Parkinsonism with Pleomorphic Pathology
Top Cited Papers
- 1 November 2004
- Vol. 44 (4) , 601-607
- https://doi.org/10.1016/j.neuron.2004.11.005
Abstract
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This publication has 30 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 diseasePublished by Elsevier ,2004
- Hereditary Early-Onset Parkinson's Disease Caused by Mutations in PINK1Science, 2004
- The PARK8 Locus in Autosomal Dominant Parkinsonism: Confirmation of Linkage and Further Delineation of the Disease-Containing IntervalAmerican Journal of Human Genetics, 2004
- α-Synuclein Locus Triplication Causes Parkinson's DiseaseScience, 2003
- Significant Linkage of Parkinson Disease to Chromosome 2q36-37American Journal of Human Genetics, 2003
- The leucine-rich repeat as a protein recognition motifPublished by Elsevier ,2001
- Protein Tyrosine Kinase Structure and FunctionAnnual Review of Biochemistry, 2000
- Fine Mapping of the Chromosome 12 Late-Onset Alzheimer Disease Locus: Potential Genetic and Phenotypic HeterogeneityAmerican Journal of Human Genetics, 2000
- Mutation in the α-Synuclein Gene Identified in Families with Parkinson's DiseaseScience, 1997