1. Both gain‐of‐function and loss‐of‐function de novo CACNA1A mutations cause severe developmental epileptic encephalopathies in the spectrum of Lennox‐Gastaut syndrome. (29th August 2019) Authors: Jiang, Xiao; Raju, Praveen K.; D'Avanzo, Nazzareno; Lachance, Mathieu; Pepin, Julie; Dubeau, François; Mitchell, Wendy G.; Bello‐Espinosa, Luis E.; Pierson, Tyler M.; Minassian, Berge A.; Lacaille, Jean‐Claude; Rossignol, Elsa Journal: Epilepsia Issue: Volume 60:issue 9(2019) Page Start: 1881 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗