Project Details
Description
Trailing Parkinson’s disease and tremor, dystonias are the third most prevalent movement disorder.
DYT1 is the most common hereditary movement disorder for which there are few, if any, good
therapeutic options. This proposal will use a new dystonic mouse model of DYT1 to explore how the
mutations associated with DYT1 cause dystonia.
| Status | Finished |
|---|---|
| Effective start/end date | 12/1/17 → 11/30/22 |
Funding
- National Institute of Neurological Disorders and Stroke: $386,831.00
- National Institute of Neurological Disorders and Stroke: $460,304.00
- National Institute of Neurological Disorders and Stroke: $414,275.00
- National Institute of Neurological Disorders and Stroke: $73,473.00
- National Institute of Neurological Disorders and Stroke: $414,274.00
- National Institute of Neurological Disorders and Stroke: $460,304.00
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