Variants in the SK2 channel gene (KCNN2) lead to dominant neurodevelopmental movement disorders
Authors: Fanny Mochel; Agnès Rastetter; Berten Ceulemans; Konrad Platzer; Sandra Yang; Deepali N Shinde; Katherine L Helbig; Diego Lopergolo; Francesca Mari; Alessandra Renieri; Elisa Benetti; Roberto Canitano; Quinten Waisfisz; Astrid S Plomp; Sylvia A Huisman; Golder N Wilson; Sara S Cathey; Raymond J Louie; Daniela Del Gaudio; Darrel Waggoner; Shawn Kacker; Kimberly M Nugent; Elizabeth R Roeder; Ange-Line Bruel; Julien Thevenon; Nadja Ehmke; Denise Horn; Manuel Holtgrewe; Frank J Kaiser; Susanne B Kamphausen; Rami Abou Jamra; Sarah Weckhuysen; Christel Depienne; Carine Dalle
Collaborators: Amsterdam University Medical Center; Antwerp University Hospital; Azienda Ospedaliera Universitaria Senese; Baylor College of Medicine; Berlin Institute of Health; Center for Molecular Neurology, VIB; Charité - Universitätsmedizin Berlin; Children's Hospital of Philadelphia; CHU Dijon Bourgogne; GeneDx; Greenwood Genetic Center; Inserm; La Pitié-Salpêtrière Hospital; Leipzig University; Prinsenstichting; Sorbonne Universités, Paris, France; Texas Tech University Health Science Center; University Hospital Magdeburg; University of Antwerp; University of Chicago; University of Duisburg-Essen; University of Siena; Vrije Universiteit Amsterdam