APA (7th ed.) Citation

Jiao, J., Zhang, H., Zhou, X., Tian, S., Gao, L., Li, B., . . . Liao, W. (2025). Missense variants in SLC9A6 cause partial epilepsy without neurodevelopmental delay. Orphanet Journal of Rare Diseases, 20(1), 1. https://doi.org/10.1186/s13023-025-03924-9

Chicago Style (17th ed.) Citation

Jiao, Jun-Ping, et al. "Missense Variants in SLC9A6 Cause Partial Epilepsy Without Neurodevelopmental Delay." Orphanet Journal of Rare Diseases 20, no. 1 (2025): 1. https://doi.org/10.1186/s13023-025-03924-9.

MLA (9th ed.) Citation

Jiao, Jun-Ping, et al. "Missense Variants in SLC9A6 Cause Partial Epilepsy Without Neurodevelopmental Delay." Orphanet Journal of Rare Diseases, vol. 20, no. 1, 2025, p. 1, https://doi.org/10.1186/s13023-025-03924-9.