Moller, R. S., Kovel, C. G. F. de, Syrbe, S., Schonewolf-Greulich, B., Rokkjaer, M., Svaneby, D., Larsen, L. H. G., Brilstra, E. H., Verbeek, N., Kerr, B., Dubbs, H., Bayat, A., Desai, S., Naidu, S., Srivastava, S., Caglayan, H., Yis, U., Saunders, C., Rook, M., Plugge, S., Jayaraman, V., Rajagopalan, R., Goldberg, E., Marsh, E., Kessler, S., Bergqvist, C., Conlin, L., Krock, B., Thiffault, I., Pendziwiat, M., Helbig, I., Polster, T., Borggräfe, I., Lemke, J. R., Boogaardt, M.-J. van den, Gardella, E. and Köleman, B. P. C.
(2017):
KCNB1 mutations are causing a neurodevelopmental disorder including epilepsy and autism.
In: Epilepsia, Vol. 58: S31-S31
| Item Type: | Journal article |
|---|---|
| Faculties: | Medicine |
| Subjects: | 600 Technology > 610 Medicine and health |
| ISSN: | 0013-9580 |
| Language: | English |
| Item ID: | 52260 |
| Date Deposited: | 14. Jun 2018 09:49 |
| Last Modified: | 14. Jun 2018 09:49 |
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