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Restricted accessResearch articleFirst published July, 2013

A Homozygous Deletion in GRID2 Causes a Human Phenotype With Cerebellar Ataxia and Atrophy

G. Eda Utine, Göknur Haliloğlu, Bilge Salancı [...]

Journal of Child Neurology

Restricted accessResearch articleFirst published August, 2021

Association of Gene Variations in Ionotropic Glutamate Receptor and Attention-Deficit/Hyperactivity Disorder in the Chinese Population: A Two-Stage Case–Control Study

Qi Zhang, Xin Huang, Xin-Zhen Chen [...]

Journal of Attention Disorders

Open accessIn briefFirst published 2017

A Rare Syndrome of GRID2 Deletion in 2 Siblings

Aravindhan Veerapandiyan, Stephanie Enner, Venkatraman Thulasi [...]

Child Neurology Open

Restricted accessResearch articleFirst published 2018

A Genetic Study of Psychosis in Huntington’s Disease: Evidence for the Involvement of Glutamate Signaling Pathways

Debby W. Tsuang, Tiffany A. Greenwood, Suman Jayadev [...]

Journal of Huntington's Disease

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Articles (4)

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1-4 of 4 results for GRID2

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Restricted accessResearch articleFirst published July, 2013

A Homozygous Deletion in GRID2 Causes a Human Phenotype With Cerebellar Ataxia and Atrophy

G. Eda Utine, Göknur Haliloğlu, Bilge Salancı [...]

Journal of Child Neurology

Restricted accessResearch articleFirst published August, 2021

Association of Gene Variations in Ionotropic Glutamate Receptor and Attention-Deficit/Hyperactivity Disorder in the Chinese Population: A Two-Stage Case–Control Study

Qi Zhang, Xin Huang, Xin-Zhen Chen [...]

Journal of Attention Disorders

Open accessIn briefFirst published 2017

A Rare Syndrome of GRID2 Deletion in 2 Siblings

Aravindhan Veerapandiyan, Stephanie Enner, Venkatraman Thulasi [...]

Child Neurology Open

Restricted accessResearch articleFirst published 2018

A Genetic Study of Psychosis in Huntington’s Disease: Evidence for the Involvement of Glutamate Signaling Pathways

Debby W. Tsuang, Tiffany A. Greenwood, Suman Jayadev [...]

Journal of Huntington's Disease