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Article

Two patients with a GRIN2A mutation and childhood-onset epilepsy.

Pediatric neurology - 1 Dec 2013

DeVries Seth P, Patel Anup D

Abstract excerpt

BACKGROUND: N-methyl-D-aspartate is a key neurotransmitter within the central nervous system and its dysfunction can play an important role in epilepsy. Mutations of genes involving the N-methyl-D-aspartate receptor have been implicated in a wide variety of neuropsychiatric disorders including epilepsy, specifically, within the glutamate receptor ionotropic N-methyl-D-aspartate 2A (GRIN2A). PATIENTS: We report...

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Source

Identifiers

PMID: 24125812
DOI: 10.1016/j.pediatrneurol.2013.08.023

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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