Delineating the GRIN1 phenotypic spectrum: A distinct genetic NMDA receptor 
encephalopathy

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.; Misceo, D.; Frengen, E.; Stromme, P.; Dlugos, D. J.; Doherty, E. S.; Bijlsma, E. K.; Ruivenkamp, C. A.; Hoffer, M. J.; Goldstein, A.; Rajan, D. S.; Narayanan, V.; Ramsey, K.; Belnap, N.; Schrauwen, I.; Richholt, R.; Koeleman, B. P.; Sa, J.; Mendonca, C.; De Kovel, Carolien G. F.; Weckhuysen, S.; Hardies, K.; De Jonghe, P.; De Meirleir, L.; 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.

doi:10.1212/wnl.0000000000002740

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Delineating the GRIN1 phenotypic spectrum: A distinct genetic NMDA receptor encephalopathy

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http://www.neurology.org/content/86/23/2171/suppl/DC1
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Neurology-2016-Lemke-2171-8.pdf
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Lemke, J. R., Geider, K., Helbig, K. L., Heyne, H. O., Schutz, H., Hentschel, J., et al. (2016). Delineating the GRIN1 phenotypic spectrum: A distinct genetic NMDA receptor encephalopathy. Neurology, 86(23), 2171-2178. doi:10.1212/wnl.0000000000002740.

Cite as: https://hdl.handle.net/11858/00-001M-0000-002B-9C4D-C

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