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Mutations in GRIN2A and GRIN2B encoding regulatory subunits of NMDA receptors cause variable neurodevelopmental phenotypes
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
*Corresponding author for this work
- University Hospital Hamburg-Eppendorf
- Technical University Darmstadt
- Aix-Marseille University
- MPI Molekulare Genetik
- University of Freiburg
- Ruprecht-Karls Universität Heidelberg
- Zurich Center for Integrative Human Physiology (ZIHP)
- University of Kiel
- Centre Saint-Paul Hopital Henri Gastaut
- University of Duisburg-Essen
- Université de Liège
- University of Erlangen–Nuremberg
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