V28. KCNA2 mutations cause epileptic encephalopathy by gain- or loss-of channel function
| Autor: | 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. |
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| Zdroj: | In Clinical Neurophysiology August 2015 126(8):e80-e80 |
| Databáze: | ScienceDirect |
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