RecruitingNCT00041600
Human Epilepsy Genetics--Neuronal Migration Disorders Study
Sponsor
Harvard University Faculty of Medicine
Enrollment
3,500 participants
Start Date
Apr 1, 1996
Study Type
OBSERVATIONAL
Conditions
Summary
The purpose of this study is to identify genes responsible for epilepsy, brain malformations and disorders of human cognition.
Eligibility
Inclusion Criteria2
- Males and females of any age.
- Persons with a brain malformation or disorder of cognition (familial intellectual disability \[previously known as mental retardation\] or autism).
Exclusion Criteria1
- Persons without a brain malformation or disorder of cognition (familial intellectual disability (previously known as mental retardation\] or autism).
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Locations(1)
View Full Details on ClinicalTrials.gov
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NCT00041600
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