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)

Boston Children's Hospital, Walsh Laboratory

Boston, Massachusetts, United States

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NCT00041600


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