SCN1A overexpression, associated with a genomic region marked by a risk variant for a common epilepsy, raises seizure susceptibility

التفاصيل البيبلوغرافية
العنوان: SCN1A overexpression, associated with a genomic region marked by a risk variant for a common epilepsy, raises seizure susceptibility
المؤلفون: Katri Silvennoinen, Kinga Gawel, Despina Tsortouktzidis, Julika Pitsch, Saud Alhusaini, Karen M. J. van Loo, Richard Picardo, Zuzanna Michalak, Susanna Pagni, Helena Martins Custodio, James Mills, Christopher D. Whelan, Greig I. de Zubicaray, Katie L. McMahon, Wietske van der Ent, Karolina J. Kirstein-Smardzewska, Ettore Tiraboschi, Jonathan M. Mudge, Adam Frankish, Maria Thom, Margaret J. Wright, Paul M. Thompson, Susanne Schoch, Albert J. Becker, Camila V. Esguerra, Sanjay M. Sisodiya
المصدر: Acta Neuropathol (Berl) 144(1), 107-127 (2022). doi:10.1007/s00401-022-02429-0
Acta Neuropathologica
بيانات النشر: Springer Science and Business Media LLC, 2022.
سنة النشر: 2022
مصطلحات موضوعية: Epilepsy, Sclerosis, Genomics, Zebrafish Proteins, Hippocampus, Seizures, Febrile, Pathology and Forensic Medicine, NAV1.1 Voltage-Gated Sodium Channel, Cellular and Molecular Neuroscience, Epilepsy, Temporal Lobe, Animals, Humans, Gliosis, Neurology (clinical), Zebrafish
الوصف: Acta Neuropathol (Berl) 144(1), 107-127 (2022). doi:10.1007/s00401-022-02429-0
Published by Springer, Berlin ; Heidelberg
تدمد: 1432-0533
0001-6322
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b8d32b787b2f5ddb39c622fff671d2f6Test
https://doi.org/10.1007/s00401-022-02429-0Test
حقوق: OPEN
رقم الانضمام: edsair.doi.dedup.....b8d32b787b2f5ddb39c622fff671d2f6
قاعدة البيانات: OpenAIRE