For example, autosomal dominant lateral temporal lobe epilepsy (ADLTE) is associated with mutations in the LGI1 gene, whereas familial mesial temporal lobe epilepsy (FMTLE) encompasses various subtypes (e.g., hippocampal sclerosis, febrile seizures) but has not yet been conclusively linked to a single gene. Here, LGI1 is linked to autosomal dominant epilepsy with auditory features.