Common synaptic phenotypes arising from diverse mutations in the human NMDA receptor subunit GluN2A von Elmasri, Marwa, Hunter, Daniel William, Winchester, Giles, Bates, Ella Emine, Aziz, Wajeeha, Van Der Does, Does Moolenaar, Karachaliou, Eirini, Sakimura, Kenji, Penn, Andrew. Charles

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