Cita APA

Wengert, E. R., Tronhjem, C. E., Wagnon, J. L., Johannesen, K. M., Petit, H., Krey, I., . . . Møller, R. S. (2019). Biallelic inherited SCN8A variants, a rare cause of SCN8A-related developmental and epileptic encephalopathy. Epilepsia.

Citación estilo Chicago

Wengert, Eric R., et al. "Biallelic Inherited SCN8A Variants, a Rare Cause of SCN8A-related Developmental and Epileptic Encephalopathy." Epilepsia 2019.

Cita MLA

Wengert, Eric R., et al. "Biallelic Inherited SCN8A Variants, a Rare Cause of SCN8A-related Developmental and Epileptic Encephalopathy." Epilepsia 2019.