APA (7th ed.) Citation

Stringer, R. N., Jurkovicova-Tarabova, B., Souza, I. A., Ibrahim, J., Vacik, T., Fathalla, W. M., . . . Weiss, N. (2021). De novo SCN8A and inherited rare CACNA1H variants associated with severe developmental and epileptic encephalopathy. Molecular Brain, 14(1), 1. https://doi.org/10.1186/s13041-021-00838-y

Chicago Style (17th ed.) Citation

Stringer, Robin N., et al. "De Novo SCN8A and Inherited Rare CACNA1H Variants Associated with Severe Developmental and Epileptic Encephalopathy." Molecular Brain 14, no. 1 (2021): 1. https://doi.org/10.1186/s13041-021-00838-y.

MLA (9th ed.) Citation

Stringer, Robin N., et al. "De Novo SCN8A and Inherited Rare CACNA1H Variants Associated with Severe Developmental and Epileptic Encephalopathy." Molecular Brain, vol. 14, no. 1, 2021, p. 1, https://doi.org/10.1186/s13041-021-00838-y.