APA (7th ed.) Citation

Pujol‐Giménez, J., Mirzaa, G., Blue, E. E., Albano, G., Miller, D. E., Allworth, A., . . . Raskind, W. H. (2023). Dominant‐negative variant in SLC1A4 causes an autosomal dominant epilepsy syndrome. Annals of Clinical & Translational Neurology, 10(6), 1046. https://doi.org/10.1002/acn3.51786

Chicago Style (17th ed.) Citation

Pujol‐Giménez, Jonai, et al. "Dominant‐negative Variant in SLC1A4 Causes an Autosomal Dominant Epilepsy Syndrome." Annals of Clinical & Translational Neurology 10, no. 6 (2023): 1046. https://doi.org/10.1002/acn3.51786.

MLA (9th ed.) Citation

Pujol‐Giménez, Jonai, et al. "Dominant‐negative Variant in SLC1A4 Causes an Autosomal Dominant Epilepsy Syndrome." Annals of Clinical & Translational Neurology, vol. 10, no. 6, 2023, p. 1046, https://doi.org/10.1002/acn3.51786.

Warning: These citations may not always be 100% accurate.