SCN1B encephalopathy [OMIM: 617350, EIEE52] is a DEE caused by homozygous missense or splicing mutations in SCN1B (Patino et al., 2009; Ogiwara et al., 2012). Show abstract Ion Channels Involvement in Neurodevelopmental Disorders 2020, Neuroscience Citation Excerpt : As for Kv1.1, mutations...