Cerebellar Dysfunction in DYT1

Project: Research project

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.
StatusActive
Effective start/end date12/1/1711/30/22

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: $414,274.00
  • National Institute of Neurological Disorders and Stroke: $73,473.00
  • National Institute of Neurological Disorders and Stroke: $460,304.00

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.