Electrophysiological characterization of a Cav3.2 calcium channel missense variant associated with epilepsy and hearing loss

T-type calcium channelopathies encompass a group of human disorders either caused or exacerbated by mutations in the genes encoding different T-type calcium channels. Recently, a new heterozygous missense muta...
Source: Molecular Brain - Category: Neuroscience Authors: Tags: Micro report Source Type: research