Delineating the GRIN1 phenotypic spectrum: A distinct genetic NMDA receptor encephalopathy
- Author(s):
- Lemke, J.R.; Geider, K.; Helbig, K.L.; Heyne, H.O.; Schutz, H.; Hentschel, J.; Courage, C.; Depienne, C.; Nava, C.; Heron, D.; Moller, R.S.; Hjalgrim, H.; Lal, D.; Neubauer, B.A.; Nurnberg, P.; Thiele, H.; Kurlemann, G.; Arnold, G.L.; Bhambhani, V.; Bartholdi, D.; Pedurupillay, C.R.J.; Misceo, D.; Frengen, E.; Stromme, P.; Dlugos, D.J.; Doherty, E.S.; Bijlsma, E.K.; Ruivenkamp, C.A.; Hoffer, M.J.V. (0000-0002-1812-7670); Goldstein, A.; Rajan, D.S.; Narayanan, V.; Ramsey, K.; Belnap, N.; Schrauwen, I.; Richholt, R.; Koeleman, B.P.C.; Sa, J.; Mendonca, C.; Kovel, C.G.F. de; Weckhuysen, S.; Hardies, K.; Jonghe, P. de; Meirleir, L. de; Milh, M.; Badens, C.; Lebrun, M.; Busa, T.; Francannet, C.; Piton, A.; Riesch, E.; Biskup, S.; Vogt, H.; Dorn, T.; Helbig, I.; Michaud, J.L.; Laube, B.; Syrbe, S.
- Published
- 2016
- Publication type
- Article / Letter to editor
- Date issued
- 2016-06-07
- Language
- English
- Is part of
- Neurology (2016), Vol. 86, no. 23, p. 2171-2178
- hdl
- 1887/112961
- doi
- 10.1212/WNL.0000000000002740