Population genetic approaches to neurological disease: Parkinson's disease as an example.
Ontology highlight
ABSTRACT: Parkinson's disease (PD) is a common, progressive, incurable disabling condition. The cause is unknown but over the past few years tremendous progress in our understanding of the genetic bases of this condition has been made. To date, this has almost exclusively come from the study of relatively rare Mendelian forms of the disease and there are no currently, widely accepted common variants known to increase susceptibility. The role that the "Mendelian" genes play in common sporadic forms of PD is unknown. Moreover, most studies in PD can really be described as candidate polymorphism studies rather than true and complete assessments of the genes themselves. We provide a model of how one might tackle some of these issues using Parkinson's disease as an illustration. One of the emerging hypot
SUBMITTER: Gandhi S
PROVIDER: S-EPMC1569523 | biostudies-literature | 2005 Aug
REPOSITORIES: biostudies-literature
ACCESS DATA