(Q34086321)

30 July 2017

title

Genetic variation of the human glycine receptor subunit genes GLRA3 and GLRB and susceptibility to idiopathic generalized epilepsies (English)

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30 July 2017

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Sobetzko D

1

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30 July 2017

Sander T

series ordinal

2

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30 July 2017

Becker CM

series ordinal

3

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30 July 2017

publication date

1 August 2001

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American Journal of Medical Genetics Part A

30 July 2017

published in

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30 July 2017

volume

105

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30 July 2017

issue

6

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30 July 2017

page(s)

534-538

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Concepts of absence epilepsies: discrete syndromes or biological continuum?

30 July 2017

cites work

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Mutation of the Ca2+ channel beta subunit gene Cchb4 is associated with ataxia and seizures in the lethargic (lh) mouse

21 January 2018

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

21 January 2018

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Proposal for revised classification of epilepsies and epileptic syndromes. Commission on Classification and Terminology of the International League Against Epilepsy

21 January 2018

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Sodium/hydrogen exchanger gene defect in slow-wave epilepsy mutant mice.

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Mutations of SCN1A, encoding a neuronal sodium channel, in two families with GEFS+2

21 January 2018

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Absence epilepsy in tottering mutant mice is associated with calcium channel defects

21 January 2018

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The human glycine receptor beta subunit: primary structure, functional characterisation and chromosomal localisation of the human and murine genes

21 January 2018

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Incidence of epilepsy and unprovoked seizures in Rochester, Minnesota: 1935-1984.

21 January 2018

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The idiopathic generalized epilepsies of adolescence with childhood and juvenile age of onset

21 January 2018

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The frameshift mutation oscillator (Glra1(spd-ot)) produces a complete loss of glycine receptor alpha1-polypeptide in mouse central nervous system

21 January 2018

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The mouse stargazer gene encodes a neuronal Ca2+-channel gamma subunit.

21 January 2018

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The human glycine receptor beta subunit gene (GLRB): structure, refined chromosomal localization, and population polymorphism

21 January 2018

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The spastic mouse: aberrant splicing of glycine receptor beta subunit mRNA caused by intronic insertion of L1 element

21 January 2018

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The human glycine receptor subunit alpha3. Glra3 gene structure, chromosomal localization, and functional characterization of alternative transcripts

21 January 2018

1 reference

21 January 2018

Targeting epilepsy genes

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What's wrong with Bonferroni adjustments

21 January 2018

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Ion channels and the genetic contribution to epilepsy

21 January 2018

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The genetics of idiopathic generalized epilepsy: implications for the understanding of its aetiology

21 January 2018

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Association analysis of sequence variants of GABA(A) alpha6, beta2, and gamma2 gene cluster and alcohol dependence.

21 January 2018

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Point mutation of glycine receptor alpha 1 subunit in the spasmodic mouse affects agonist responses

21 January 2018

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Mutations in the alpha 1 subunit of the inhibitory glycine receptor cause the dominant neurologic disorder, hyperekplexia

21 January 2018

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

21 January 2018

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

21 January 2018

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21 January 2018

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21 January 2018

Identifiers

DOI

10.1002/AJMG.1488

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30 July 2017

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