Počet záznamů: 1
De novo SCN8A and inherited rare CACNA1H variants associated with severe developmental and epileptic encephalopathy
- 1.Stringer, R. N., Jurkovicova-Tarabova, B., Souza, I. A., Ibrahim, J., Vacík, T., Fathalla, W. M., Hertecant, J., Zamponi, G. W., Lacinová, L., Weiss, N. De novo SCN8A and inherited rare CACNA1H variants associated with severe developmental and epileptic encephalopathy. Molecular Brain. 2021, 14(1), 126. E-ISSN 1756-6606. Dostupné z: doi: 10.1186/s13041-021-00838-y.
Počet záznamů: 1