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APA Citation
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. (2019). recurrent SLC1A2 variants cause epilepsy via a dominant negative mechanism. Annals of neurology, 85(6), 921–926. http://access.bl.uk/ark:/81055/vdc_100083291938.0x000051