1. A spontaneous missense mutation in the chromodomain helicase DNA‐binding protein 8 (CHD8) gene: a novel association with congenital myasthenic syndrome. (7th May 2020) Authors: Lee, C. Y.; Petkova, M.; Morales‐Gonzalez, S.; Gimber, N.; Schmoranzer, J.; Meisel, A.; Böhmerle, W.; Stenzel, W.; Schuelke, M.; Schwarz, J. M. Journal: Neuropathology & applied neurobiology Issue: Volume 46:Number 6(2020) Page Start: 588 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗