| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 6016497 | European Journal of Paediatric Neurology | 2016 | 5 Pages |
Abstract
Hence, epilepsy is not a mandatory feature of patients with a STXBP1 mutation.
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Authors
Janina Gburek-Augustat, Stefanie Beck-Woedl, Andreas Tzschach, Peter Bauer, Martin Schoening, Angelika Riess,