CHAPEL HILL, NC - The gene UBE3A plays a critical role in early neurological development. If UBE3A is overexpressed - or if the enzymatic function of UBE3A protein is hyperactive - autism ensues. A lack of functional UBE3A causes Angelman syndrome (AS), a neurodevelopmental disorder characterized by severe developmental delay, motor deficits, absence of speech, and, in most cases, epilepsy. Prevention of seizures in AS model mice by restoring UBE3A after birth has proved largely unsuccessful, indicating that the timing of gene expression is also important.