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GRID2 gene

Known as: GRID2, GLUTAMATE RECEPTOR, IONOTROPIC, DELTA 2, GluR-delta-2 
 
National Institutes of Health

Papers overview

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2019
2019
Key Clinical Message Different mutations in glutamate receptor ionotropic delta 2 (GRID2) gene cause cerebellar ataxia in human… Expand
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2016
2016
Autism is one of the most common subtypes of autism spectrum disorder (ASD). Recent studies suggested a relationship between… Expand
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2015
2015
Purpose:The aim of this study was to identify the genetic cause of early-onset autosomal recessive cerebellar ataxia associated… Expand
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2014
2014
Abstract Mevalonate kinase deficiency (MKD) is a rare autosomal disease caused by mutations in the mevalonate kinase gene (MVK… Expand
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2014
2014
Spinocerebellar degenerations (SCDs) are a large class of sporadic or hereditary neurodegenerative disorders characterized by… Expand
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2013
2013
GRID2 is a member of the ionotropic glutamate receptor family of excitatory neurotransmitter receptors. GRID2 encodes the… Expand
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2007
2007
Mouse genetic studies have identified several genes involved in cerebellar development. The mouse mutants staggerer and lurcher… Expand
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Highly Cited
2004
Highly Cited
2004
Fragile sites are classified as common or rare depending on their occurrence in the populations. While rare sites are mainly… Expand
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2003
2003
The Lurcher mutation transforms the GRID2 receptor into a constitutively opened channel. In Lurcher heterozygous mice, cerebellar… Expand
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2003
2003
The orphan glutamate receptor delta2 is selectively expressed in Purkinje cells and plays a crucial role in cerebellar functions… Expand
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