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. 2021 Nov 4;108(11):2206. doi: 10.1016/j.ajhg.2021.09.018

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 Innes, Xing-Chang Wei, Boris Keren, Cyril Mignot, Robert Roger Lebel, Steven M Sperber, Ai Sakonju, Nienke Dosa, Daniela QCM Barge-Schaapveld, Cacha MPCD Peeters-Scholte, Claudia AL 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 ∗
PMCID: PMC8595928  PMID: 34739836

(The American Journal of Human Genetics 108, 1692–1709; September 2, 2021)

In the originally published version of this article, individuals with the c.1969G>A (p.Ala657Thr) variant were mistakenly identified as homozygous in the summary. They are heterozygous, and this has been corrected online. The authors regret this error.

Articles from American Journal of Human Genetics are provided here courtesy of American Society of Human Genetics

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