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Annals of Clinical and Translational Neurology|September 5, 2015
PRIMA1 mutation: a new cause of nocturnal frontal lobe epilepsyMichael S Hildebrand, Rick Tankard, Elena V Gazina, et al.Neurology|December 3, 2017
Clinical and molecular characterization of KCNT1-related severe early-onset epilepsyAmy McTague, Umesh Nair, Sony Malhotra, et al.Trends in Neurosciences|April 26, 2018
Progress in Understanding and Treating SCN2A-Mediated DisordersStephan J Sanders, Arthur J Campbell, Jeffrey R Cottrell, et al.Brain : a Journal of Neurology|April 22, 2026
Collapse of feed-forward inhibition underpins hyperexcitability in GABAA gain-of-function epilepsyChaseley E McKenzie, Khaing Phyu Aung, Altair Brito Dos Santos, et al.Annals of Neurology|April 6, 2017
Myoclonus epilepsy and ataxia due to KCNC1 mutation: Analysis of 20 cases and K+ channel propertiesKaren L Oliver, Silvana Franceschetti, Carol J Milligan, et al.Circulation|July 15, 2021
Therapeutic Inhibition of Acid-Sensing Ion Channel 1a Recovers Heart Function After Ischemia-Reperfusion InjuryMeredith A Redd, Sarah E Scheuer, Natalie J Saez, et al.Nature Genetics|November 18, 2014
A recurrent de novo mutation in KCNC1 causes progressive myoclonus epilepsyMikko Muona, Samuel F Berkovic, Leanne M Dibbens, et al.The Lancet. Neurology|July 24, 2018
Rare coding variants in genes encoding GABAA receptors in genetic generalised epilepsies: an exome-based case-control studyPatrick May, Simon Girard, Merle Harrer, et al.Pageof 19