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Article

Systematic screening for mutations in the human N-methyl-D-aspartate receptor 1 gene in schizophrenic patients from the German population.

Psychiatric genetics - 1 Dec 2004

Paus Sebastian, Rietschel Marcella, Schulze Thomas G, Ohlraun Stephanie, Diaconu Carmen C, Van Den Bogaert Ann, Maier Wolfgang, Propping Peter, Cichon Sven, Nöthen Markus M

Abstract excerpt

Evidence for a dysfunction of the N-methyl-D-aspartate (NMDA) type of ionotropic glutamate receptors in schizophrenic patients, comes from neurochemical and clinical pharmacologic data. Therefore, the NMDAR1 gene can be regarded as an interesting candidate gene for schizophrenia. Several groups h...

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Identifiers

PMID: 15564900
DOI: 10.1097/00041444-200412000-00013

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-15564900-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

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