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.
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.
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.
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.
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.
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