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Common synaptic phenotypes arising from diverse mutations in the human NMDA receptor subunit GluN2A. (2022)

First Author: Elmasri M

Attributed to: GLUTAMATE RECEPTOR ION CHANNELS AND SYNAPSE DYSFUNCTION funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1038/s42003-022-03115-3

PubMed Identifier: 35228668

Publication URI: http://europepmc.org/abstract/MED/35228668

Type: Journal Article/Review

Volume: 5

Parent Publication: Communications biology

Issue: 1

ISSN: 2399-3642