Pathogenic Cav3.2 channel mutation in a child with primary generalized epilepsy

Overview of attention for article published in Molecular Brain, October 2019

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Gain of function in CaV3.2 mutations and primary generalized #epilepsy in 6yr old child. Mutation R1282W (red dot) caused increase in current density; A1765V (green dot) saw no increase. #iochannels https://t.co/AgSL5GFt1y https://t.co/qriGydJZBW

New Short Report: Pathogenic Cav3.2 channel mutation in a child with primary generalized epilepsy https://t.co/gosfX2s1sn

RT @TheWeissLab: New T-type calcium channel mutations identified in a child with primary generalized #epilepsy. #ionchannels #channelopathi…

RT @TheWeissLab: New T-type calcium channel mutations identified in a child with primary generalized #epilepsy. #ionchannels #channelopathi…

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