Common synaptic phenotypes arising from diverse mutations in the human NMDA receptor subunit GluN2A (2020)

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/10.1101/2020.08.06.240010

Publication URI: http://dx.doi.org/10.1101/2020.08.06.240010

Type: Preprint