Project Details
Description
PROJECT SUMMARY/ABSTRACT
The goal of this proposal is to define the signature phenotypic profiles of the two most
common genetically defined forms of early onset Parkinson[unreadable]s Disease (PD), parkin (Park2) and
glucocerebrosidase (GBA), cross-sectionally (Aim 1), longitudinally (Aim 2), and before motor
manifestations that define PD occur (Aim 3). We will recruit 75 PD probands who carry parkin
mutations, 100 PD probands who carry GBA mutations, and 100 noncarrier (idiopathic PD)
probands and their first-degree relatives (3 per family). The majority of these families have
participated in the Consortium on Risk for Early Onset PD (CORE PD) study, which has enrolled
1062 PD probands with age at onset (AAO)
Status | Finished |
---|---|
Effective start/end date | 9/30/10 → 11/30/13 |
Funding
- National Institute of Neurological Disorders and Stroke: US$500,000.00
ASJC Scopus Subject Areas
- Genetics
- Epidemiology
- Clinical Neurology
- Neurology
Fingerprint
Explore the research topics touched on by this project. These labels are generated based on the underlying awards/grants. Together they form a unique fingerprint.