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ROLE OF Ca-ACTIVATED K CHANNELS AND Na,K-ATPase IN PROSTAGLANDIN E- AND E-IND...
International audience -
A TASK3 channel (KCNK9) mutation in a genetic model of absence epilepsy.
Childhood absence epilepsy is an idiopathic, generalized, nonconvulsive epilepsy with a multifactorial genetic etiology. The KCNK9 gene coding for the TASK3 (Twik-like...
