Table 1.

Human K⁺ channelepsies.

The table depicts the principal inherited human channelepsies caused by mutations in K⁺ channel α subunits or associated accessory proteins. For each channelepsy, information about the name of the mutated gene/protein, its expression in brain regions relevant to the pathology, type of epilepsy and association with other known syndromes, and dysfunction in channel behavior caused by the mutations are reported.