Genetic Study of Familial Epilepsy
NCT00006059 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 898
Last updated 2005-06-24
Summary
OBJECTIVES:
I. Determine the chromosomal regions that contain genes that raise the risk of epilepsy in families by performing genetic linkage analysis of idiopathic/cryptogenic epilepsy.
Conditions
Sponsors & Collaborators
- collaborator OTHER
-
National Center for Research Resources (NCRR)
lead NIH
Principal Investigators
-
Ruth Ottman · Columbia University
Eligibility
- Min Age
- 0 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 1997-01-31
Countries
- United States
Study Locations
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