Referenced in: none

Automatically associated channels: Cav3.2 , Kv10.1

Title: Effects of Cav3.2 channel mutations linked to idiopathic generalized epilepsy.

Authors: Houman Khosravani, Christopher Bladen, David B Parker, Terrance P Snutch, John E McRory, Gerald W Zamponi

Journal, date & volume: Ann. Neurol., 2005 May , 57, 745-9

PubMed link: http://www.ncbi.nlm.nih.gov/pubmed/15852375

Abstract
Heron and colleagues (Ann Neurol 2004;55:595-596) identified three missense mutations in the Cav3.2 T-type calcium channel gene (CACNA1H) in patients with idiopathic generalized epilepsy. None of the variants were associated with a specific epilepsy phenotype and were not found in patients with juvenile absence epilepsy or childhood absence epilepsy. Here, we introduced and functionally characterized these three mutations using transiently expressed human Cav3.2 channels. Two of the mutations exhibited functional changes that are consistent with increased channel function. Taken together, these findings along with previous reports, strongly implicate CACNA1H as a susceptibility gene in complex idiopathic generalized epilepsy.