Possible association between childhood absence epilepsy and the gene encoding GABRB3 (Q57066913)

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31 October 2019

title

Possible association between childhood absence epilepsy and the gene encoding GABRB3 (English)

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childhood absence epilepsy

31 October 2019

main subject

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4

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31 October 2019

Werner Sieghart

9

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31 October 2019

Siegfried Kasper

10

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31 October 2019

Harald Aschauer

11

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31 October 2019

author name string

M Feucht

1

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31 October 2019

K Fuchs

2

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31 October 2019

E Pichlbauer

3

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31 October 2019

J Scharfetter

5

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31 October 2019

R Goessler

6

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31 October 2019

T Füreder

7

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31 October 2019

N Cvetkovic

8

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31 October 2019

language of work or name

English

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publication date

1 October 1999

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31 October 2019

published in

Biological Psychiatry

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31 October 2019

volume

46

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31 October 2019

issue

7

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31 October 2019

page(s)

997-1002

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Developmental changes in human gamma-aminobutyric acidA receptor subunit composition.

31 October 2019

cites work

1 reference

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Duplication of the 15q11-13 region in a patient with autism, epilepsy and ataxia.

7 January 2021

1 reference

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

7 January 2021

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Myoclonic absence-like seizures and chromosome abnormality syndromes

7 January 2021

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The Human γ-Aminobutyric Acid Receptor Subunit β3 and α5 Gene Cluster in Chromosome 15q11-q13 Is Rich in Highly Polymorphic (CA)n Repeats

7 January 2021

1 reference

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Structure and organization of GABRB3 and GABRA5.

7 January 2021

1 reference

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Lack of association between juvenile myoclonic epilepsy and GABRA5 and GABRB3 genes

7 January 2021

1 reference

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Mice devoid of gamma-aminobutyrate type A receptor beta3 subunit have epilepsy, cleft palate, and hypersensitive behavior

7 January 2021

1 reference

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7 January 2021

GABAA receptor channels

1 reference

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Tests for linkage and association in nuclear families

7 January 2021

1 reference

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A cluster of three GABAA receptor subunit genes is deleted in a neurological mutant of the mouse p locus.

7 January 2021

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Stargazer: a new neurological mutant on chromosome 15 in the mouse with prolonged cortical seizures.

7 January 2021

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7 January 2021

Targeting epilepsy genes

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7 January 2021

GABA and epileptogenesis

1 reference

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Differential and transient expression of GABAA receptor alpha-subunit mRNAs in the developing rat CNS

7 January 2021

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The phenotypic spectrum related to the human epilepsy susceptibility gene "EJM1"

7 January 2021

1 reference

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Refinement of map position of the human GluR6 kainate receptor gene (GRIK2) and lack of association and linkage with idiopathic generalized epilepsies

7 January 2021

1 reference

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Common subtypes of idiopathic generalized epilepsies: lack of linkage to D20S19 close to candidate loci (EBN1, EEGV1) on chromosome 20

7 January 2021

1 reference

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Exclusion of linkage between idiopathic generalized epilepsies and the GABAA receptor alpha 1 and gamma 2 subunit gene cluster on chromosome 5.

7 January 2021

1 reference

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Multiplicity of GABAA--benzodiazepine receptors.

7 January 2021

1 reference

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GABAA receptors: ligand-gated Cl- ion channels modulated by multiple drug-binding sites

7 January 2021

1 reference

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Identification of a putative DNA replication origin in the gamma-aminobutyric acid receptor subunit beta3 and alpha5 gene cluster on human chromosome 15q11-q13, a region associated with parental imprinting and allele-specific replication timing.

7 January 2021

1 reference

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GABAA receptor impairment in the genetic absence epilepsy rats from Strasbourg (GAERS): an immunocytochemical and receptor binding autoradiographic study.

7 January 2021

1 reference

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

7 January 2021

1 reference

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A novel allosteric modulatory site on the GABAA receptor beta subunit

7 January 2021

1 reference

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Angelman syndrome: consensus for diagnostic criteria. Angelman Syndrome Foundation

7 January 2021

1 reference

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10.1016/S0006-3223(99)00039-6

7 January 2021

Identifiers

DOI

1 reference

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31 October 2019

1 reference