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 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, Carine Dalle, Christel Depienne
Brain. 2020 Dec 1;143(12):3564-3573. doi: 10.1093/brain/awaa346.
https://pubmed.ncbi.nlm.nih.gov/33242881/

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