Genetic variation of the human glycine receptor subunit genes GLRA3 and GLRB and susceptibility to idiopathic generalized epilepsies (Q34086321)

30 July 2017

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

1 reference

30 July 2017

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Sobetzko D

1

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PubMed ID

11496371

30 July 2017

Sander T

series ordinal

2

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PubMed ID

11496371

30 July 2017

Becker CM

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3

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30 July 2017

1 August 2001

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American Journal of Medical Genetics Part A

30 July 2017

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30 July 2017

105

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30 July 2017

534-538

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30 July 2017

6

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Concepts of absence epilepsies: discrete syndromes or biological continuum?

30 July 2017

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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

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

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

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

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

1 reference

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

1 reference

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

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

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

1 reference

30 July 2017

1 reference

PubMed ID

11496371