Genotype/Phenotype Correlation of Movement Disorders and Other Neurological Diseases
NCT00001667 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 300
Last updated 2008-03-04
Summary
The purpose of this protocol is to identify families with inherited neurologic conditions, especially movement disorders, to evaluate affected and unaffected individuals clinically, and to obtain blood samples for genetic analysis.
Conditions
- Movement Disorders
- Myoclonus
- Nervous System Diseases
- Tic Disorders
- Tremor
Sponsors & Collaborators
-
National Institute of Neurological Disorders and Stroke (NINDS)
lead NIH
Eligibility
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 1997-03-31
- Completion
- 2000-04-30
Countries
- United States
Study Locations
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