Delineating SPTAN1 associated phenotypes: from isolated epilepsy to encephalopathy with progressive brain atrophy
The genetic basis of epileptic encephalopathies is increasingly recognised. Syrbe et al. define the role of SPTAN1 in childhood-onset epilepsies. In the largest
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| Main Authors: | , , , |
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| Format: | Article (Journal) |
| Language: | English |
| Published: |
2017
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| In: |
Brain
Year: 2017, Volume: 140, Issue: 9, Pages: 2322-2336 |
| ISSN: | 1460-2156 |
| DOI: | 10.1093/brain/awx195 |
| Online Access: | Verlag, kostenfrei, Volltext: http://dx.doi.org/10.1093/brain/awx195 Verlag, Volltext: https://academic.oup.com/brain/article/140/9/2322/4096697 
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| Author Notes: | Steffen Syrbe, Frederike L. Harms, Elena Parrini, Martino Montomoli, Ulrike Mütze, Katherine L. Helbig, Tilman Polster, Beate Albrecht, Ulrich Bernbeck, Ellen van Binsbergen, Saskia Biskup, Lydie Burglen, Jonas Denecke, Bénédicte Heron, Henrike O. Heyne, Georg F. Hoffmann, Frauke Hornemann, Takeshi Matsushige, Ryuki Matsuura, Mitsuhiro Kato, G. Christoph Korenke, Alma Kuechler, Constanze Lämmer, Andreas Merkenschlager, Cyril Mignot, Susanne Ruf, Mitsuko Nakashima, Hirotomo Saitsu, Hannah Stamberger, Tiziana Pisano, Jun Tohyama, Sarah Weckhuysen, Wendy Werckx, Julia Wickert, Francesco Mari, Nienke E. Verbeek, Rikke S. Møller, Bobby Koeleman, Naomichi Matsumoto, William B. Dobyns, Domenica Battaglia, Johannes R. Lemke, Kerstin Kutsche and Renzo Guerrini |
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