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Charzewska, A., Maiwald, R., Kahrizi, K., Oehl‐Jaschkowitz, B., Dufke, A., Lemke, J.R., Enders, H., Najmabadi, H., Tzschach, A., Hachmann, W., Jensen, C., Bienek, M., Poznański, J., Nawara, M., Chilarska, T., Obersztyn, E., Hoffman‐Zacharska, D., Gos, M., Bal, J., Kalscheuer, V.M.
Published in Clinical genetics (01.11.2018)
Published in Clinical genetics (01.11.2018)
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V28. KCNA2 mutations cause epileptic encephalopathy by gain- or loss-of channel function
Hedrich, U.B.S, Syrbe, S, Riesch, E, Djémié, T, Müller, S, Møller, R.S, Maher, B, Hernandez-Hernandez, L, Synofzik, M, Caglayan, H.S, Arslan, M, Serratosa, J, Gonzalez, M, Züchner, S, Palotie, A, Suls, A, De Jonghe, P, Helbig, I, Biskup, S, Wolff, M, Maljevic, S, Schuele-Freyer, R, Sisodiya, S.M, Weckhuysen, S, Lerche, H, Lemke, J.R
Published in Clinical neurophysiology (01.08.2015)
Published in Clinical neurophysiology (01.08.2015)
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Hentschel, J., Sändig, I., Unger, T., Lemke, J.R., Wittekind, C.
Published in Forum (Heidelberg) (01.03.2015)
Published in Forum (Heidelberg) (01.03.2015)
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