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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