Referenced in: none

Automatically associated channels: ClC2 , ClC4

Title: Mutations in the CLCN2 gene are a rare cause of idiopathic generalized epilepsy syndromes.

Authors: E Stogmann, P Lichtner, C Baumgartner, M Schmied, C Hotzy, F Asmus, F Leutmezer, S Bonelli, E Assem-Hilger, K Vass, K Hatala, T M Strom, T Meitinger, F Zimprich, A Zimprich

Journal, date & volume: Neurogenetics, 2006 Nov , 7, 265-8

PubMed link: http://www.ncbi.nlm.nih.gov/pubmed/16932951

Abstract