Clustered mutations in the GRIK2 kainate receptor subunit gene underlie diverse neurodevelopmental disorders

Jacob R. Stolz, Kendall M. Foote, Hermine E. Veenstra-Knol, Rolph Pfundt, Sanne W. ten Broeke, Nicole de Leeuw, Laura Roht, Sander Pajusalu, Reelika Part, Ionella Rebane, Katrin Õunap, Zornitza Stark, Edwin P. Kirk, John A. Lawson, Sebastian Lunke, John Christodoulou, Raymond J. Louie, R. Curtis Rogers, Jessica M. Davis, A. Micheil InnesXing Chang Wei, Boris Keren, Cyril Mignot, Robert Roger Lebel, Steven M. Sperber, Ai Sakonju, Nienke Dosa, Daniela Q.C.M. Barge-Schaapveld, Cacha M.P.C.D. Peeters-Scholte, Claudia A.L. Ruivenkamp, Bregje W. van Bon, Joanna Kennedy, Karen J. Low, Sian Ellard, Lewis Pang, Joseph J. Junewick, Paul R. Mark, Gemma L. Carvill, Geoffrey T. Swanson*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

19 Scopus citations

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Keyphrases

Neuroscience

Biochemistry, Genetics and Molecular Biology