Mutations in the sodium-gated potassium channel subunit gene KCNT1 are associated to different phenotypes such as Epilepsy of Infancy with Migrating Focal Seizures (EIMFS), Autosomal Dominant Sleep-related Hypermotor Epilepsy (ADSHE), previously named Nocturnal Frontal Lobe Epilepsy (ADNFLE), and other forms of focal epilepsies, epileptic encephalopathies and intellectual disabilities [1].

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