Association between variation in the human KCNJ10 potassium ion channel gene and seizure susceptibility
- 29 February 2004
- journal article
- research article
- Published by Elsevier in Epilepsy Research
- Vol. 58 (2-3), 175-183
- https://doi.org/10.1016/j.eplepsyres.2004.02.003
Abstract
No abstract availableKeywords
This publication has 43 references indexed in Scilit:
- Suggestive evidence for association of two potassium channel genes with different idiopathic generalised epilepsy syndromesEpilepsy Research, 2002
- Lack of Association Between an Interleukin 1 Beta (IL‐1β) Gene Variation and Refractory Temporal Lobe EpilepsyEpilepsia, 2001
- First genetic evidence of GABAA receptor dysfunction in epilepsy: a mutation in the γ2-subunit geneNature Genetics, 2001
- A Novel SCN1A Mutation Associated with Generalized Epilepsy with Febrile Seizures Plus—and Prevalence of Variants in Patients with EpilepsyAmerican Journal of Human Genetics, 2001
- The nicotinic receptor β2 subunit is mutant in nocturnal frontal lobe epilepsyNature Genetics, 2000
- Lack of association between temporal lobe epilepsy and a novel polymorphism in the alpha 2 subunit gene (ATP1A2) of the sodium potassium transporting ATPaseAmerican Journal of Medical Genetics, 2000
- Mapping Loci for Pentylenetetrazol-Induced Seizure Susceptibility in MiceJournal of Neuroscience, 1999
- Classifications of the International League Against Epilepsy: Time for ReappraisalEpilepsia, 1998
- A pore mutation in a novel KQT-like potassium channel gene in an idiopathic epilepsy familyNature Genetics, 1998
- Mapping murine loci for seizure response to kainic acidMammalian Genome, 1997