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Liu, D. GRIN2A Gene. Encyclopedia. Available online: https://encyclopedia.pub/entry/3819 (accessed on 28 September 2026).
Liu D. GRIN2A Gene. Encyclopedia. Available at: https://encyclopedia.pub/entry/3819. Accessed September 28, 2026.
Liu, Dean. "GRIN2A Gene" Encyclopedia, https://encyclopedia.pub/entry/3819 (accessed September 28, 2026).
Liu, D. (2020, December 22). GRIN2A Gene. In Encyclopedia. https://encyclopedia.pub/entry/3819
Liu, Dean. "GRIN2A Gene." Encyclopedia. Web. 22 December, 2020.
GRIN2A Gene
Edit

Glutamate ionotropic receptor NMDA type subunit 2A

genes

References

  1. Burnashev N, Szepetowski P. NMDA receptor subunit mutations inneurodevelopmental disorders. Curr Opin Pharmacol. 2015 Feb;20:73-82. doi:10.1016/j.coph.2014.11.008.
  2. Carvill GL, Regan BM, Yendle SC, O'Roak BJ, Lozovaya N, Bruneau N, BurnashevN, Khan A, Cook J, Geraghty E, Sadleir LG, Turner SJ, Tsai MH, Webster R, OuvrierR, Damiano JA, Berkovic SF, Shendure J, Hildebrand MS, Szepetowski P, SchefferIE, Mefford HC. GRIN2A mutations cause epilepsy-aphasia spectrum disorders. NatGenet. 2013 Sep;45(9):1073-6. doi: 10.1038/ng.2727.
  3. Lemke JR, Lal D, Reinthaler EM, Steiner I, Nothnagel M, Alber M, Geider K,Laube B, Schwake M, Finsterwalder K, Franke A, Schilhabel M, Jähn JA, Muhle H,Boor R, Van Paesschen W, Caraballo R, Fejerman N, Weckhuysen S, De Jonghe P,Larsen J, Møller RS, Hjalgrim H, Addis L, Tang S, Hughes E, Pal DK, Veri K, VaherU, Talvik T, Dimova P, Guerrero López R, Serratosa JM, Linnankivi T, LehesjokiAE, Ruf S, Wolff M, Buerki S, Wohlrab G, Kroell J, Datta AN, Fiedler B, KurlemannG, Kluger G, Hahn A, Haberlandt DE, Kutzer C, Sperner J, Becker F, Weber YG,Feucht M, Steinböck H, Neophythou B, Ronen GM, Gruber-Sedlmayr U, Geldner J,Harvey RJ, Hoffmann P, Herms S, Altmüller J, Toliat MR, Thiele H, Nürnberg P,Wilhelm C, Stephani U, Helbig I, Lerche H, Zimprich F, Neubauer BA, Biskup S, vonSpiczak S. Mutations in GRIN2A cause idiopathic focal epilepsy with rolandicspikes. Nat Genet. 2013 Sep;45(9):1067-72. doi: 10.1038/ng.2728.
  4. Lesca G, Rudolf G, Bruneau N, Lozovaya N, Labalme A, Boutry-Kryza N, Salmi M, Tsintsadze T, Addis L, Motte J, Wright S, Tsintsadze V, Michel A, Doummar D,Lascelles K, Strug L, Waters P, de Bellescize J, Vrielynck P, de Saint Martin A, Ville D, Ryvlin P, Arzimanoglou A, Hirsch E, Vincent A, Pal D, Burnashev N,Sanlaville D, Szepetowski P. GRIN2A mutations in acquired epileptic aphasia andrelated childhood focal epilepsies and encephalopathies with speech and language dysfunction. Nat Genet. 2013 Sep;45(9):1061-6. doi: 10.1038/ng.2726.
  5. Paoletti P. Molecular basis of NMDA receptor functional diversity. Eur JNeurosci. 2011 Apr;33(8):1351-65. doi: 10.1111/j.1460-9568.2011.07628.x.
  6. Reutlinger C, Helbig I, Gawelczyk B, Subero JI, Tönnies H, Muhle H,Finsterwalder K, Vermeer S, Pfundt R, Sperner J, Stefanova I, Gillessen-Kaesbach G, von Spiczak S, van Baalen A, Boor R, Siebert R, Stephani U, Caliebe A.Deletions in 16p13 including GRIN2A in patients with intellectual disability,various dysmorphic features, and seizure disorders of the rolandic region.Epilepsia. 2010 Sep;51(9):1870-3. doi: 10.1111/j.1528-1167.2010.02555.x.
  7. Turner SJ, Mayes AK, Verhoeven A, Mandelstam SA, Morgan AT, Scheffer IE.GRIN2A: an aptly named gene for speech dysfunction. Neurology. 2015 Feb10;84(6):586-93. doi: 10.1212/WNL.0000000000001228.
  8. Wyllie DJ, Livesey MR, Hardingham GE. Influence of GluN2 subunit identity onNMDA receptor function. Neuropharmacology. 2013 Nov;74:4-17. doi:10.1016/j.neuropharm.2013.01.016.
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