PubMed 20890276
Referenced in: none
Automatically associated channels: Slo1
Title: Mutations in GRIN2A and GRIN2B encoding regulatory subunits of NMDA receptors cause variable neurodevelopmental phenotypes.
Authors: Sabine Endele, Georg Rosenberger, Kirsten Geider, Bernt Popp, Ceyhun Tamer, Irina Stefanova, Mathieu Milh, Fanny Kortüm, Angela Fritsch, Friederike K Pientka, Yorck Hellenbroich, Vera M Kalscheuer, Jürgen Kohlhase, Ute Moog, Gudrun Rappold, Anita Rauch, Hans-Hilger Ropers, Sarah von Spiczak, Holger Tönnies, Nathalie Villeneuve, Laurent Villard, Bernhard Zabel, Martin Zenker, Bodo Laube, André Reis, Dagmar Wieczorek, Lionel Van Maldergem, Kerstin Kutsche
Journal, date & volume: Nat. Genet., 2010 Nov , 42, 1021-6
PubMed link: http://www.ncbi.nlm.nih.gov/pubmed/20890276
Abstract