APA

Stergachis A. B., Pujol-Giménez J., Gyimesi G., Fuster D., Albano G., Troxler M., Picker J., Rosenberg P. A., Bergin A., Peters J., El Achkar C. M., Harini C., Manzi S., Rotenberg A., Hediger M. A. & Rodan L. H. (20200330). Recurrent SLC1A2 variants cause epilepsy via a dominant negative mechanism. : Annals of neurology.

Chicago

Stergachis Andrew B, Pujol-Giménez Jonai, Gyimesi Gergely, Fuster Daniel, Albano Giusppe, Troxler Marina, Picker Jonathan, Rosenberg Paul A, Bergin Ann, Peters Jurriaan, El Achkar Christelle Moufawad, Harini Chellamani, Manzi Shannon, Rotenberg Alexander, Hediger Matthias A and Rodan Lance H. 20200330. Recurrent SLC1A2 variants cause epilepsy via a dominant negative mechanism. : Annals of neurology.

Harvard

Stergachis A. B., Pujol-Giménez J., Gyimesi G., Fuster D., Albano G., Troxler M., Picker J., Rosenberg P. A., Bergin A., Peters J., El Achkar C. M., Harini C., Manzi S., Rotenberg A., Hediger M. A. and Rodan L. H. (20200330). Recurrent SLC1A2 variants cause epilepsy via a dominant negative mechanism. : Annals of neurology.

MLA

Stergachis Andrew B, Pujol-Giménez Jonai, Gyimesi Gergely, Fuster Daniel, Albano Giusppe, Troxler Marina, Picker Jonathan, Rosenberg Paul A, Bergin Ann, Peters Jurriaan, El Achkar Christelle Moufawad, Harini Chellamani, Manzi Shannon, Rotenberg Alexander, Hediger Matthias A and Rodan Lance H. Recurrent SLC1A2 variants cause epilepsy via a dominant negative mechanism. : Annals of neurology. 20200330.