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 acid-sensitive K

Data and Resources

Additional Info

Field Value
Source ISSN: 0895-8696
Author Holter, J., Carter, D., Leresche, N., Crunelli, V., Vincent, P.
Maintainer CCSD
Last Updated May 9, 2026, 16:48 (UTC)
Created May 9, 2026, 16:48 (UTC)
Identifier hal-00086355
Language en
contributor Research laboratory ; Cardiff University-School of Biosciences
creator Holter, J.
date 2005-05-09T00:00:00
harvest_object_id 92db992e-5713-46cb-ad21-1dc2cd787f13
harvest_source_id 3374d638-d20b-4672-ba96-a23232d55657
harvest_source_title test moissonnage SELUNE
metadata_modified 2025-04-14T00:00:00
set_spec type:ART