Clustered mutations in the GRIK2 kainate receptor subunit gene underlie diverse neurodevelopmental disorders (vol 108, pg 1692, 2021)

Stolz, J.R.; Foote, K.M.; Veenstra-Knol, H.E.; Pfundt, R.; Broeke, S.W. ten; Leeuw, N. de; ... ; Swanson, G.T. (2021)

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• All authors: Stolz, J.R.; Foote, K.M.; Veenstra-Knol, H.E.; Pfundt, R.; Broeke, S.W. ten; Leeuw, N. de; Roht, L.; Pajusalu, S.; Part, R.; Rebane, I.; Ounap, K.; Stark, Z.; Kirk, E.P.; Lawson, J.A.; Lunke, S.; Christodoulou, J.; Louie, R.J.; Rogers, R.C.; Davis, J.M.; Innes, A.M.; Wei, X.C.; Keren, B.; Mignot, C.; Lebel, R.R.; Sperber, S.M.; Sakonju, A.; Dosa, N.; Barge-Schaapveld, D.Q.C.M.; Peeters-Scholte, C.M.P.C.D.; Ruivenkamp, C.A.L.; Bon, B.W. van; Kennedy, J.; Low, K.J.; Ellard, S.; Pang, L.W.; Junewick, J.J.; Mark, P.R.; Carvill, G.L.; Swanson, G.T.
• Date: 2021-11-04
• Title of host publication: American Journal of Human Genetics
• Volume: 108
• Issue: 11
• Pages: 2206 - 2206
• DOI: doi:10.1016/j.ajhg.2021.09.018
• Link: http://www.cell.com/article/S0002929721003542/pdf