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Common synaptic phenotypes arising from diverse mutations in the human NMDA receptor subunit GluN2A.
Commun Biol. 2022 Feb 28;5(1):174. doi: 10.1038/s42003-022-03115-3.
Commun Biol. 2022.
PMID: 35228668
Free PMC article.
Synaptic Dysfunction by Mutations in GRIN2B: Influence of Triheteromeric NMDA Receptors on Gain-of-Function and Loss-of-Function Mutant Classification.
Elmasri M, Lotti JS, Aziz W, Steele OG, Karachaliou E, Sakimura K, Hansen KB, Penn AC.
Elmasri M, et al. Among authors: karachaliou e.
Brain Sci. 2022 Jun 15;12(6):789. doi: 10.3390/brainsci12060789.
Brain Sci. 2022.
PMID: 35741674
Free PMC article.
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