SCN1A overexpression, associated with a genomic region marked by a risk variant for a common epilepsy, raises seizure susceptibility
| Autor: | Silvennoinen, Katri, Gawel, Kinga Aurelia, Tsortouktzidis, Despina, Pitsch, Julika, Alhusaini, Saud, van Loo, Karen M. J., Picardo, Richard, Michalak, Zuzanna, Pagni, Susanna, Martins Custodio, Helena, Mills, James, Whelan, Christopher D., de Zubicaray, Greig I., McMahon, Katie L., van der Ent, Wietske, Kirstein-Smardzewska, Karolina Joanna, Tiraboschi, Ettore, Mudge, Jonathan M., Frankish, Adam, Thom, Maria, Wright, Margaret J., Thompson, Paul M., Schoch, Susanne, Becker, Albert J., Esguerra, Camila, Sisodiya, Sanjay M. |
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| Zdroj: | Silvennoinen, Katri Gawel, Kinga Aurelia Tsortouktzidis, Despina Pitsch, Julika Alhusaini, Saud van Loo, Karen M. J. Picardo, Richard Michalak, Zuzanna Pagni, Susanna Martins Custodio, Helena Mills, James Whelan, Christopher D. de Zubicaray, Greig I. McMahon, Katie L. van der Ent, Wietske Kirstein-Smardzewska, Karolina Joanna Tiraboschi, Ettore Mudge, Jonathan M. Frankish, Adam Thom, Maria Wright, Margaret J. Thompson, Paul M. Schoch, Susanne Becker, Albert J. Esguerra, Camila Sisodiya, Sanjay M. . SCN1A overexpression, associated with a genomic region marked by a risk variant for a common epilepsy, raises seizure susceptibility. Acta Neuropathologica. 2022, 144(1), 107-127 Acta Neuropathologica |
| Databáze: | NORA (Norwegian Open Research Archive) |
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