De novo loss-or gain-of-function mutations in KCNA2 cause epileptic encephalopathy

Nishizaki, Steffen;Hedrich, Ulrike B. S.;Riesch, Erik;Djémié, Tania;Müller, Stephan;Møller, Rikke S.;Maher, Bridget;Hernandez-Hernandez, Laura;Synofzik, Matthis;Caglayan, Hande S.;Arslan, Mutluay;Serratosa, José M.;Nothnagel, Michael;May, Patrick;Krause, Roland;Löffler, Heidrun;Detert, Katja;Dorn, Thomas;Vogt, Heinrich;Krämer, Günter;Schöls, Ludger;Mullis, Primus E.;Linnankivi, Tarja;Lehesjoki, Anna-Elina;Sterbova, Katalin;Craiu, Dana C.;Hoffman-Zacharska, Dorota;Korff, Christian M.;Weber, Yvonne G.;Steinlin, Maja;Gallati, Sabina;Bertsche, Astrid;Bernhard, Matthias K.;Merkenschlager, Andreas;Kiess, Wieland;Gonzalez, Michael;Züchner, Stephan;Palotie, Aarno;Suls, Arvid;De Jonghe, Peter;Helbig, Ingo;Biskup, Saskia;Wolff, Markus;Maljevic, Snezana;Schüle, Rebecca;Striano Pasquale;Sisodiya;Sanjay M.;Zara Federico;Weckhuysen, Sarah;Lerche, Holger;Lemke, Johannes R.

2015-01-01