PRRT2 Mutations Cause Benign Familial Infantile Epilepsy and Infantile Convulsions with Choreoathetosis Syndrome

Overview of attention for article published in American Journal of Human Genetics, January 2012

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Gene and mutations thereof associated with seizure and movement disorders

Grant US-11473143-B2

United States of America

Gene and mutations thereof associated with seizure and movement disorders

Grant US-9752193-B2

United States of America

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