| Literature DB >> 11163549 |
A A Bolonna1, R W Kerwin, J Munro, M J Arranz, A J Makoff.
Abstract
A dysfunctional glutamatergic system has been implicated in the pathophysiology of schizophrenia. The group III metabotropic glutamate receptor (mGluR) types 7 and 8 presynaptically inhibit glutamate release, thereby modulating glutamatergic transmission in the brain. We conducted association studies to investigate the novel Tyr433Phe (mGluR7) variant and the 2846-C/T (mGluR8) polymorphism in schizophrenia. Both variants, present at high frequencies, failed to demonstrate any significant association with schizophrenia (mGluR7 [Tyr433Phe] allele: P=0.33; genotype: P=0.63; mGluR8 [2846-C/T] allele: P=0.72; genotype: P=0.63).Entities:
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Year: 2001 PMID: 11163549 DOI: 10.1016/s0920-9964(99)00235-2
Source DB: PubMed Journal: Schizophr Res ISSN: 0920-9964 Impact factor: 4.939