Variants in the SK2 channel gene (KCNN2) lead to dominant neurodevelopmental movement disorders

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 WaggonerShawn 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, Carine Dalle, Christel Depienne*

*Corresponding author for this work

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Medicine & Life Sciences