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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1992 1
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1994 1
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1996 1
2016 1
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2018 1
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2024 1

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PubMed for id: 2328705310

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Page 1
Disease-associated nonsense and frame-shift variants resulting in the truncation of the GluN2A or GluN2B C-terminal domain decrease NMDAR surface expression and reduce potentiating effects of neurosteroids.
Kysilov B, Kuchtiak V, Hrcka Krausova B, Balik A, Korinek M, Fili K, Dobrovolski M, Abramova V, Chodounska H, Kudova E, Bozikova P, Cerny J, Smejkalova T, Vyklicky L. Kysilov B, et al. Cell Mol Life Sci. 2024 Jan 12;81(1):36. doi: 10.1007/s00018-023-05062-6. Cell Mol Life Sci. 2024. PMID: 38214768 Free PMC article.
GRIN2B-Related Neurodevelopmental Disorder.
Platzer K, Lemke JR. Platzer K, et al. 2018 May 31 [updated 2021 Mar 25]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. 2018 May 31 [updated 2021 Mar 25]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. PMID: 29851452 Free Books & Documents. Review.
Human GRIN2B variants in neurodevelopmental disorders.
Hu C, Chen W, Myers SJ, Yuan H, Traynelis SF. Hu C, et al. J Pharmacol Sci. 2016 Oct;132(2):115-121. doi: 10.1016/j.jphs.2016.10.002. Epub 2016 Oct 19. J Pharmacol Sci. 2016. PMID: 27818011 Free PMC article. Review.