Associated Papers
Damaging coding variants within kainate receptor channel genes are enriched in individuals with schizophrenia, autism and intellectual disabilities.
Koromina M et al.
Scientific Reports, 2019
31844109 (PubMed )
Supplement: 41598_2019_55635_MOESM1_ESM.pdf
Sequencing of the GRIK1 gene in patients with juvenile absence epilepsy does not reveal mutations affecting receptor structure.
Izzi C et al.
American Journal of Medical Genetics, 2002
Association study of polymorphisms in the GluR5 kainate receptor gene (GRIK1) with schizophrenia.
Shibata H et al.
Psychiatric Genetics, 2001
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