Personalized structural biology reveals the molecular mechanisms underlying heterogeneous epileptic phenotypes caused by de novo KCNC2 variants. Human Genetics and Genomics Advances, (3)4:100131, 2022. [PUMA: developmental variant, disease molecular encephalopathy, electrophysiology, Diseases simulations, personalized structural rare dynamics interpretation, epileptic KCNC2, and topic_lifescience DEE, variant Network, Undiagnosed biology,] URL