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Study identifier: NCT00041600 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Human Epilepsy Genetics--Neuronal Migration Disorders Study

Condition: Brain Malformation · Neuronal Migration Disorder · Cognition Disorder  ·  Sponsor: Harvard University Faculty of Medicine

PhaseN/A
Planned participants3500
Who can joinAll sexes, N/A to no upper limit
Healthy volunteersNo

About this study

The purpose of this study is to identify genes responsible for epilepsy, brain malformations and disorders of human cognition.

This description comes directly from the study's public registry record.

Talk to the study team

Jennifer Neil, MS  ·  617-919-2865  ·  walshresearch@childrens.harvard.edu

Abbe Lai, MS  ·  617-919-4371

Always discuss trial participation with your own doctor first.

Locations (1)

Boston Children's Hospital, Walsh LaboratoryBoston, Massachusetts, United StatesRecruiting

Follow this study

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Source record: clinicaltrials.gov/study/NCT00041600