Human Epilepsy Genetics--Neuronal Migration Disorders Study
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
AgeNot listed
SponsorHarvard University Faculty of Medicine
About this trial
The purpose of this study is to identify genes responsible for epilepsy, brain malformations and disorders of human cognition.
Eligibility criteria
Qualifiers
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).
Persons without a brain malformation or disorder of cognition (familial intellectual disability (previously known as mental retardation] or autism).
Disqualifiers
None
Trial design
Treatments tested in this trial
- Not listed
Trial groups
No trial groups listed
Locations
1Boston Children's Hospital, Walsh Laboratory02115, BostonMassachusetts, United States
Sponsors and collaborators
Harvard University Faculty of Medicine
Lead sponsor
National Institute of Neurological Disorders and Stroke (NINDS)
Collaborator
Howard Hughes Medical Institute
Collaborator
Source ClinicalTrials.gov