α-Synuclein missense and multiplication mutations in autosomal dominant Parkinson’s disease
- 26 August 2004
- journal article
- research article
- Published by Elsevier in Neuroscience Letters
- Vol. 367 (1) , 97-100
- https://doi.org/10.1016/j.neulet.2004.05.100
Abstract
No abstract availableKeywords
This publication has 18 references indexed in Scilit:
- Comparison of kindreds with parkinsonism and α‐synuclein genomic multiplicationsAnnals of Neurology, 2004
- Molecular Pathways of Neurodegeneration in Parkinson's DiseaseScience, 2003
- Functional analysis of intra-allelic variation at NACP-Rep1 in the ?-synuclein geneHuman Genetics, 2003
- ESEfinder: a web resource to identify exonic splicing enhancersNucleic Acids Research, 2003
- Two large Polish kindreds with levodopa-responsive Parkinsonism not linked to known Parkinsonian genes and loci.Parkinsonism & Related Disorders, 2003
- Large French-Canadian family with Lewy body parkinsonism: Exclusion of known lociMovement Disorders, 2002
- Effect of allelic variation at the NACP-Rep1 repeat upstream of the alpha-synuclein gene (SNCA) on transcription in a cell culture luciferase reporter systemHuman Molecular Genetics, 2001
- alpha-synuclein gene haplotypes are associated with Parkinson's diseaseHuman Molecular Genetics, 2001
- Diagnostic Criteria for Parkinson DiseaseArchives of Neurology, 1999
- AlaSOPro mutation in the gene encoding α-synuclein in Parkinson's diseaseNature Genetics, 1998