Clustered mutations in the GRIK2 kainate receptor subunit gene underlie diverse neurodevelopmental disorders
Jacob R. Stolz(Northwestern University), Geoffrey T. Swanson(Northwestern University), Sander Pajusalu(MACOM (United States)), Boris Keren(Sorbonne Université), Joanna Kennedy(University of Exeter), Sebastian Lunke(Royal Children's Hospital), Reelika Part(Tallinn Health Care College), Rolph Pfundt(Radboud University Nijmegen), Ionella Rebane(Tallinn Health Care College), Katrin Õunap(Tartu University Hospital), Ai Sakonju(SUNY Upstate Medical University), Xing‐Chang Wei, Kendall M. Foote(Northwestern University), John A. Lawson(Universities UK), Edwin P. Kirk(The University of Sydney), John Christodoulou(The University of Melbourne), Nienke P. Dosa(SUNY Upstate Medical University), Raymond J. Louie(Greenwood Genetic Center), A. Micheil Innes(University of Calgary), Robert Roger Lebel(SUNY Upstate Medical University), Steven M. Sperber(Hackensack Meridian Health), Lewis Pang(Royal Devon & Exeter NHS Foundation Trust), Karen Low(North Bristol NHS Trust), Zornitza Stark(Zoos Victoria), Gemma L. Carvill(University of Washington), Laura Roht(Tartu University Hospital), Cyril Mignot(Sorbonne Université), Cacha Peeters‐Scholte(Leiden University Medical Center), Sanne W. ten Broeke(Leiden University Medical Center), Paul R. Mark(Spectrum Health), Daniela Q.C.M. Barge‐Schaapveld(Leiden University), Claudia Ruivenkamp(The Netherlands Cancer Institute), Sian Ellard(University of Exeter), Hermine E. Veenstra‐Knol(University Medical Center Groningen), Joseph Junewick(Helen DeVos Children's Hospital), R. Curtis Rogers(Greenwood Genetic Center), Bregje W.M. van Bon(Radboud University Nijmegen), Jessica Davis(Greenwood Genetic Center), Nicole de Leeuw(Radboud University Nijmegen)
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