A TASK3 channel (KCNK9) mutation in a genetic model of absence epilepsy. - Archive ouverte HAL Accéder directement au contenu
Article Dans Une Revue Journal of Molecular Neuroscience Année : 2005

A TASK3 channel (KCNK9) mutation in a genetic model of absence epilepsy.

Résumé

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

Domaines

Neurosciences
Fichier non déposé

Dates et versions

hal-00086355 , version 1 (18-07-2006)

Identifiants

  • HAL Id : hal-00086355 , version 1

Citer

J. Holter, D. Carter, N. Leresche, V. Crunelli, P. Vincent. A TASK3 channel (KCNK9) mutation in a genetic model of absence epilepsy.. Journal of Molecular Neuroscience, 2005, 25, pp.37-51. ⟨hal-00086355⟩
42 Consultations
0 Téléchargements

Partager

Gmail Facebook X LinkedIn More