Human Epilepsy Genetics--Neuronal Migration Disorders Study

Recruiting now

Conditions studied: Brain Malformation, Neuronal Migration Disorder, Cognition Disorder, Epilepsy

In brief

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

Key facts

Study ID

NCT00041600

Run by

Harvard University Faculty of Medicine

People needed

3500

Starts

1996-04-01

Expected to finish

2030-06-01

Last updated by the study team

2023-09-21

Who can join

Age: any. Sex: any. Healthy volunteers: not accepted.

Where it is running

• Boston Children's Hospital, Walsh Laboratory — Boston, Massachusetts, United States (enrolling)

Full record on ClinicalTrials.gov

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