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Platzer, Konrad and Yuan, Hongjie and Schütz, Hannah and Winschel, Alexander and Chen, Wenjuan and Hu, Chun and Kusumoto, Hirofumi and Heyne, Henrike O. and Helbig, Katherine L. and Tang, Sha and Willing, Marcia C. and Tinkle, Brad T. and Adams, Darius J. and Depienne, Christel and Keren, Boris and Mignot, Cyril and Frengen, Eirik and Strømme, Petter and Biskup, Saskia and Döcker, Dennis and Strom, Tim M. and Mefford, Heather C. and Myers, Candace T. and Muir, Alison M. and LaCroix, Amy and Sadleir, Lynette and Scheffer, Ingrid E. and Brilstra, Eva and van Haelst, Mieke M. and van der Smagt, Jasper J. and Bok, Levinus A. and Møller, Rikke S. and Jensen, Uffe B. and Millichap, John J. and Berg, Anne T. and Goldberg, Ethan M. and De Bie, Isabelle and Fox, Stephanie and Major, Philippe and Jones, Julie R. and Zackai, Elaine H. and Abou Jamra, Rami and Rolfs, Arndt and Leventer, Richard J. and Lawson, John A. and Roscioli, Tony and Jansen, Floor E. and Ranza, Emmanuelle and Korff, Christian M. and Lehesjoki, Anna-Elina and Courage, Carolina and Linnankivi, Tarja and Smith, Douglas R. and Stanley, Christine and Mintz, Mark and McKnight, Dianalee and Decker, Amy and Tan, Wen-Hann and Tarnopolsky, Mark A. and Brady, Lauren I. and Wolff, Markus and Dondit, Lutz and Pedro, Helio F. and Parisotto, Sarah E. and Jones, Kelly L. and Patel, Anup D. and Franz, David N. and Vanzo, Rena and Marco, Elysa and Ranells, Judith D. and Di Donato, Nataliya and Dobyns, William B. and Laube, Bodo and Traynelis, Stephen F. and Lemke, Johannes R. (2017):
GRIN2B encephalopathy: novel findings on phenotype, variant clustering, functional consequences and treatment aspects.
In: Journal of medical genetics, pp. 460-470, 54, (7), ISSN 1468-6244,
[Article]

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