Suggestive evidence for association of two potassium channel genes with different idiopathic generalised epilepsy syndromes (Q44233533)

1 December 2017

title

Suggestive evidence for association of two potassium channel genes with different idiopathic generalised epilepsy syndromes (English)

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1 December 2017

1

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1 December 2017

Osei-Lah A

2

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1 December 2017

Wilkie H

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1 December 2017

Nashef L

4

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1 December 2017

McCormick D

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1 December 2017

Asherson P

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1 December 2017

Makoff AJ

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1 December 2017

publication date

1 December 2002

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1 December 2017

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1 December 2017

volume

52

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1 December 2017

issue

2

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1 December 2017

page(s)

107-116

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Epilepsies in twins: genetics of the major epilepsy syndromes.

1 December 2017

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7 January 2021

Structural and mutational analysis of KCNQ2, the major gene locus for benign familial neonatal convulsions

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A potassium channel mutation in neonatal human epilepsy

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The role of GABAB mechanisms in animal models of absence seizures

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Association study designs for complex diseases

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A pore mutation in a novel KQT-like potassium channel gene in an idiopathic epilepsy family

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Failure to replicate association between the gene for the neuronal nicotinic acetylcholine receptor ?4 subunit (CHRNA4) and IGE

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7 January 2021

Association between the alpha(1a) calcium channel gene CACNA1A and idiopathic generalized epilepsy

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7 January 2021

Colocalization and coassembly of two human brain M-type potassium channel subunits that are mutated in epilepsy

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7 January 2021

A proposed diagnostic scheme for people with epileptic seizures and with epilepsy: report of the ILAE Task Force on Classification and Terminology

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7 January 2021

Mutation analysis of the inwardly rectifying K(+) channels KCNJ6 (GIRK2) and KCNJ3 (GIRK1) in juvenile myoclonic epilepsy

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7 January 2021

Haplotype tagging for the identification of common disease genes

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IRK(1-3) and GIRK(1-4) inwardly rectifying K+ channel mRNAs are differentially expressed in the adult rat brain

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7 January 2021

Molecular cloning of a mouse G-protein-activated K+ channel (mGIRK1) and distinct distributions of three GIRK (GIRK1, 2 and 3) mRNAs in mouse brain

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7 January 2021

Heteromultimerization of G-protein-gated inwardly rectifying K+ channel proteins GIRK1 and GIRK2 and their altered expression in weaver brain

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Universal, robust, highly quantitative SNP allele frequency measurement in DNA pools.

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Genetic case-control association studies - correcting for multiple testing

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Association studies in psychiatric genetics

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A potassium channel mutation in weaver mice implicates membrane excitability in granule cell differentiation

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Anatomical and functional aspects of mu opioid receptors in epileptic WAG/Rij rats

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Linkage disequilibrium in the human genome

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Biased tests of association: comparisons of allele frequencies when departing from Hardy-Weinberg proportions

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Normal cerebellar development but susceptibility to seizures in mice lacking G protein-coupled, inwardly rectifying K+ channel GIRK2

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7 January 2021

A novel potassium channel gene, KCNQ2, is mutated in an inherited epilepsy of newborns

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7 January 2021

A missense mutation in the neuronal nicotinic acetylcholine receptor alpha 4 subunit is associated with autosomal dominant nocturnal frontal lobe epilepsy

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7 January 2021

Possible association of a silent polymorphism in the neuronal nicotinic acetylcholine receptor subunit alpha4 with common idiopathic generalized epilepsies

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7 January 2021

Candidate-gene approaches for studying complex genetic traits: practical considerations

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7 January 2021

M-type KCNQ2-KCNQ3 potassium channels are modulated by the KCNE2 subunit

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7 January 2021

Interpretation of results from genetic studies of multifactorial diseases

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7 January 2021

KCNQ2 and KCNQ3 potassium channel subunits: molecular correlates of the M-channel

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7 January 2021

RETRACTED: Association of mu-opioid receptor subunit gene and idiopathic generalized epilepsy

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7 January 2021

10.1016/S0920-1211(02)00195-X

Identifiers

DOI

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1 December 2017

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