Erratum: Clustered mutations in the GRIK2 kainate receptor subunit gene underlie diverse neurodevelopmental disorders (The American Journal of Human Genetics (2021) 108(9) (1692–1709), (S0002929721002755), (10.1016/j.ajhg.2021.07.007))

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 journalComment/debatepeer-review

Abstract

(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.

Original languageEnglish (US)
Pages (from-to)2206
Number of pages1
JournalAmerican journal of human genetics
Volume108
Issue number11
DOIs
StatePublished - Nov 4 2021

ASJC Scopus subject areas

  • Genetics
  • Genetics(clinical)

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