KCNJ10 potassium ion channel single nucleotide polymorphism in pediatric patients with idiopathic generalized epilepsy

Author:

Dai Alper Ibrahim,Bay Ali,Gorucu Senay,Sivasli Ercan,Bosnak Mehmet

Publisher

Elsevier BV

Subject

Psychiatry and Mental health,Neurology (clinical),General Neuroscience

Reference18 articles.

1. First genetic evidence of GABA(A) receptor dysfunction in epilepsy: a mutation in the gamma2-subunit gene;Baulae;Nat Genet,2001

2. Epilepsy, ataxia, sensorineural deafness, tubulopathy, and KCNJ10 mutations;Bockenhauer;N Engl J Med,2009

3. Association between variation in the human KCNJ10 potassium ion channel gene and seizure susceptibility;Buono;Epilepsy Res,2004

4. The nicotinic receptor beta 2 subunit is mutant in noctumal frontal lobe epilepsy;De Fusco;Nat Genet,2000

5. Fine mapping of a seizure susceptibility locus on mouse chromosome 1: nomination of Kcnj10 as a causative gene, Mamm;Ferraro;Genome,2004

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