Genetic susceptibility in Parkinson's disease
- 31 July 2009
- journal article
- review article
- Published by Elsevier BV in Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease
- Vol. 1792 (7), 597-603
- https://doi.org/10.1016/j.bbadis.2008.11.008
Abstract
No abstract availableKeywords
This publication has 70 references indexed in Scilit:
- LRRK2 R1628P increases risk of Parkinson’s disease: replication evidenceHuman Genetics, 2008
- Haplotypes and gene expression implicate the MAPT region for Parkinson diseaseNeurology, 2008
- A HapMap harvest of insights into the genetics of common diseaseJCI Insight, 2008
- Sequencing analysis of OMI/HTRA2 shows previously reported pathogenic mutations in neurologically normal controlsHuman Molecular Genetics, 2008
- Complete screening for glucocerebrosidase mutations in Parkinson disease patients from PortugalNeurobiology of Aging, 2007
- A survey of genetic human cortical gene expressionNature Genetics, 2007
- Mutations in the glucocerebrosidase gene are associated with early-onset Parkinson diseaseNeurology, 2007
- Association analysis of MAPT H1 haplotype and subhaplotypes in Parkinson's diseaseAnnals of Neurology, 2007
- α-Synuclein Locus Triplication Causes Parkinson's DiseaseScience, 2003
- Occurrence of Parkinson's syndrome in type 1 Gaucher diseaseQJM: An International Journal of Medicine, 1996