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Lemke, Johannes R. and Geider, Kirsten and Helbig, Katherine L. and Heyne, Henrike O. and Schütz, Hannah and Hentschel, Julia and Courage, Carolina and Depienne, Christel and Nava, Caroline and Heron, Delphine and Møller, Rikke S. and Hjalgrim, Helle and Lal, Dennis and Neubauer, Bernd A. and Nürnberg, Peter and Thiele, Holger and Kurlemann, Gerhard and Arnold, Georgianne L. and Bhambhani, Vikas and Bartholdi, Deborah and Pedurupillay, Christeen Ramane J. and Misceo, Doriana and Frengen, Eirik and Strømme, Petter and Dlugos, Dennis J. and Doherty, Emily S. and Bijlsma, Emilia K. and Ruivenkamp, Claudia A. and Hoffer, Mariette J. V. and Goldstein, Amy and Rajan, Deepa S. and Narayanan, Vinodh and Ramsey, Keri and Belnap, Newell and Schrauwen, Isabelle and Richholt, Ryan and Koeleman, Bobby P. C. and Sá, Joaquim and Mendonça, Carla and de Kovel, Carolien G. F. and Weckhuysen, Sarah and Hardies, Katia and De Jonghe, Peter and De Meirleir, Linda and Milh, Mathieu and Badens, Catherine and Lebrun, Marine and Busa, Tiffany and Francannet, Christine and Piton, Amélie and Riesch, Erik and Biskup, Saskia and Vogt, Heinrich and Dorn, Thomas and Helbig, Ingo and Michaud, Jacques L. and Laube, Bodo and Syrbe, Steffen (2016):
Delineating the GRIN1 phenotypic spectrum: A distinct genetic NMDA receptor encephalopathy.
In: Neurology, pp. 2171-8, 86, (23), ISSN 1526-632X,
[Article]

This list was generated on Sat Nov 16 00:11:15 2019 CET.