-CNRNA4 mutations:familial frontal lobe epilepsy.

–SCN1A mutations: lots– febrile seizures to Dravet syndrome. –KCNQ2 mutations: benign familial neonatal epilepsy.

–SCN4A mutations :periodic paralysis or myotonia.

–LGI-1 mutations:autosomal dominant partial epilepsy  with auditory features