A de novo splice site mutation in <i>CASK</i> causes FG syndrome‐4 and congenital nystagmus
Peter O. Dunn(University of Wisconsin–Milwaukee), Isabelle Schrauwen, Ryan Richholt(Neurology, Inc), Keri Ramsey(Translational Genomics Research Institute), Matt De Both(Translational Genomics Research Institute), Ana M. Claasen(Translational Genomics Research Institute), Jason J. Corneveaux(Translational Genomics Research Institute), Matthew J. Huentelman(Translational Genomics Research Institute), Ashley L. Siniard(Translational Genomics Research Institute), Christopher Balak(Translational Genomics Research Institute), Vinodh Narayanan(Translational Genomics Research Institute), Szabolcs Szelinger(Translational Genomics Research Institute), John M. Opitz(University of Utah), David W. Craig(City of Hope), Newell Belnap(Translational Genomics Research Institute), George P. Prigatano(Barrow Neurological Institute), Megan Russell(Translational Genomics Research Institute), Ignazio S. Piras(University of Cagliari), Jonathan D. Roth(Rutgers, The State University of New Jersey), Sampathkumar Rangasamy(Translational Genomics Research Institute), Amanda L. Courtright(Translational Genomics Research Institute), Abby Mae Moskowitz(Translational Genomics Research Institute)
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