SYT14 and Generalized non-motor (absence) seizure: Quintero-Rivera and colleagues have demonstrated that a de novo balanced translocation t (1;3) (q32.1; q25.1) found in a 12-year old female suffering with cerebral atrophy, developmental delay and absence seizures can alter one of the SYT14 alleles, contributing to the neurodevelopmental abnormalities seen.