1. A mutation in the neonatal isoform of SCN2A causes neonatal‐onset epilepsy. Issue 3 (7th December 2021) Authors: Penkl, Anja; Reunert, Janine; Debus, Otfried M.; Homann, Anna; Och, Ulrike; Rust, Stephan; Marquardt, Thorsten Journal: American journal of medical genetics Issue: Volume 188:Issue 3(2022) Page Start: 941 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗