Study of inherited monogenic disorders in patient and tissue-specific cells

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Study of inherited monogenic disorders in patient and tissue-specific cells

Brief description of study

The purpose of this study is to learn more about the genetic mutations (changes) associated with the genes associated with neurodevelopmental disorders like epilepsy. Genes determine things about you/your child like hair and eye color, but also indicate risk for disease and responsiveness to treatment.

Clinical Study Identifier: s19-00441

Principal Investigator: Chengzu Long.

Other Investigators: Orrin Devinsky, Lei Bu, Stuart D. Katz.

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