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Published on: March 12, 2013
A TASK3 channel (KCNK9) mutation in a genetic model of absence epilepsy
Jethro Holter1, David Carter, Nathalie Leresche
1School of Bioscience, Cardiff University, Cardiff, CF10 3US, UK.
Journal of Molecular Neuroscience : MN
|March 23, 2005
Abstract:
Childhood absence epilepsy is an idiopathic, generalized, nonconvulsive epilepsy with a multifactorial genetic etiology. The KCNK9 gene coding for the TASK3 (Twik-like acid-sensitive K

