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Genotype/Phenotype Correlation of Movement Disorders and Other Neurological Diseases

Nervous System Diseases Clinical Trial

Official title:
Genotype/Phenotype Correlation of Movement Disorders and Other Neurological Diseases

Clinical Trial 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.

Clinical Trial Description

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. ;

Study Design

N/A

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT00001667
Study type Observational
Source National Institutes of Health Clinical Center (CC)
Contact
Status Completed
Phase N/A
Start date March 1997
Completion date April 2000
View Details
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