The purpose of this study is to identify and genomically-characterize individuals with genetically unexplained neurodevelopmental disorders, such as epilepsy. The overarching goal is to provide patients with improved information about the underlying genetic basis of their disorder and illuminate novel genetically-defined treatment approaches in the future.
Thank you for your interest, but this study is not currently enrolling.
Senyene Hunter
Neurology
Clinical or Medical
Observational
Developmental
Genetics and Genetic Disorders
Rare Diseases
20-3103
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