A mutation in the neonatal isoform of SCN2A causes neonatal‐onset epilepsy.

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Bibliographic Details
Title: A mutation in the neonatal isoform of SCN2A causes neonatal‐onset epilepsy.
Authors: Penkl, Anja1, Reunert, Janine1, Debus, Otfried M.2, Homann, Anna3, Och, Ulrike1, Rust, Stephan1, Marquardt, Thorsten1, marquat@uni-muenster.de
Source: American Journal of Medical Genetics. Part A; Mar2022, Vol. 188 Issue 3, p941-947, 7p
Database: Applied Science & Technology Source
Description
ISSN:15524825
DOI:10.1002/ajmg.a.62581