Entrez Id: |
2893 |
Gene Symbol: |
GRIA4 |
GRIA4
|
Movement Disorders
|
0.100 |
GeneticVariation |
CLINVAR |
Unexplained early onset epileptic encephalopathy: Exome screening and phenotype expansion.
|
26648591 |
2016 |
Entrez Id: |
2893 |
Gene Symbol: |
GRIA4 |
GRIA4
|
Movement Disorders
|
0.100 |
GeneticVariation |
CLINVAR |
High prevalence of genetic alterations in early-onset epileptic encephalopathies associated with infantile movement disorders.
|
26482601 |
2016 |
Entrez Id: |
2893 |
Gene Symbol: |
GRIA4 |
GRIA4
|
Movement Disorders
|
0.100 |
GeneticVariation |
CLINVAR |
GRIN1 mutations cause encephalopathy with infantile-onset epilepsy, and hyperkinetic and stereotyped movement disorders.
|
25864721 |
2015 |
Entrez Id: |
2893 |
Gene Symbol: |
GRIA4 |
GRIA4
|
Movement Disorders
|
0.100 |
GeneticVariation |
CLINVAR |
X-exome sequencing in Finnish families with intellectual disability--four novel mutations and two novel syndromic phenotypes.
|
24721225 |
2014 |
Entrez Id: |
2893 |
Gene Symbol: |
GRIA4 |
GRIA4
|
Movement Disorders
|
0.100 |
GeneticVariation |
CLINVAR |
Efficient strategy for the molecular diagnosis of intellectual disability using targeted high-throughput sequencing.
|
25167861 |
2014 |
Entrez Id: |
2893 |
Gene Symbol: |
GRIA4 |
GRIA4
|
Movement Disorders
|
0.100 |
GeneticVariation |
CLINVAR |
De novo mutations in epileptic encephalopathies.
|
23934111 |
2013 |
Entrez Id: |
2893 |
Gene Symbol: |
GRIA4 |
GRIA4
|
Movement Disorders
|
0.100 |
GeneticVariation |
CLINVAR |
A new mode of corticothalamic transmission revealed in the Gria4(-/-) model of absence epilepsy.
|
21857658 |
2011 |
Entrez Id: |
2893 |
Gene Symbol: |
GRIA4 |
GRIA4
|
Movement Disorders
|
0.100 |
GeneticVariation |
CLINVAR |
Excess of de novo deleterious mutations in genes associated with glutamatergic systems in nonsyndromic intellectual disability.
|
21376300 |
2011 |
Entrez Id: |
2893 |
Gene Symbol: |
GRIA4 |
GRIA4
|
Movement Disorders
|
0.100 |
GeneticVariation |
CLINVAR |
Glutamate receptor ion channels: structure, regulation, and function.
|
20716669 |
2010 |
Entrez Id: |
2893 |
Gene Symbol: |
GRIA4 |
GRIA4
|
Movement Disorders
|
0.100 |
GeneticVariation |
CLINVAR |
Glutamate receptors on myelinated spinal cord axons: II. AMPA and GluR5 receptors.
|
19224531 |
2009 |
Entrez Id: |
2893 |
Gene Symbol: |
GRIA4 |
GRIA4
|
Movement Disorders
|
0.100 |
GeneticVariation |
CLINVAR |
X-ray structure, symmetry and mechanism of an AMPA-subtype glutamate receptor.
|
19946266 |
2009 |
Entrez Id: |
2893 |
Gene Symbol: |
GRIA4 |
GRIA4
|
Movement Disorders
|
0.100 |
GeneticVariation |
CLINVAR |
Atypical functional properties of GluK3-containing kainate receptors.
|
20007474 |
2009 |
Entrez Id: |
2893 |
Gene Symbol: |
GRIA4 |
GRIA4
|
Movement Disorders
|
0.100 |
GeneticVariation |
CLINVAR |
Absence seizures in C3H/HeJ and knockout mice caused by mutation of the AMPA receptor subunit Gria4.
|
18316356 |
2008 |
Entrez Id: |
2893 |
Gene Symbol: |
GRIA4 |
GRIA4
|
Movement Disorders
|
0.100 |
GeneticVariation |
CLINVAR |
Mutations in ionotropic AMPA receptor 3 alter channel properties and are associated with moderate cognitive impairment in humans.
|
17989220 |
2007 |
Entrez Id: |
2893 |
Gene Symbol: |
GRIA4 |
GRIA4
|
Movement Disorders
|
0.100 |
GeneticVariation |
CLINVAR |
NMDA-NR1 and AMPA-GluR4 receptor subunit immunoreactivities in the absence epileptic WAG/Rij rat.
|
16487682 |
2006 |
Entrez Id: |
2893 |
Gene Symbol: |
GRIA4 |
GRIA4
|
Movement Disorders
|
0.100 |
GeneticVariation |
CLINVAR |
Extracellular vestibule determinants of Ca2+ influx in Ca2+-permeable AMPA receptor channels.
|
12692178 |
2003 |
Entrez Id: |
2893 |
Gene Symbol: |
GRIA4 |
GRIA4
|
Movement Disorders
|
0.100 |
GeneticVariation |
CLINVAR |
Glia-synapse interaction through Ca2+-permeable AMPA receptors in Bergmann glia.
|
11340205 |
2001 |
Entrez Id: |
2893 |
Gene Symbol: |
GRIA4 |
GRIA4
|
Movement Disorders
|
0.100 |
GeneticVariation |
CLINVAR |
Postnatal synaptic potentiation: delivery of GluR4-containing AMPA receptors by spontaneous activity.
|
11036266 |
2000 |
Entrez Id: |
2893 |
Gene Symbol: |
GRIA4 |
GRIA4
|
Movement Disorders
|
0.100 |
GeneticVariation |
CLINVAR |
The differential expression of 16 NMDA and non-NMDA receptor subunits in the rat spinal cord and in periaqueductal gray.
|
8254358 |
1993 |
Entrez Id: |
2893 |
Gene Symbol: |
GRIA4 |
GRIA4
|
Movement Disorders
|
0.100 |
GeneticVariation |
CLINVAR |
Light and electron immunocytochemical localization of AMPA-selective glutamate receptors in the rat brain.
|
1374769 |
1992 |