Variants in the SK2 channel gene (KCNN2) lead to dominant neurodevelopmental movement disorders (vol 143, pg 3564, 2020)
Fanny Mochel, AgnSs 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(2023)
AI 理解论文
溯源树
样例