APA (7th ed.) Citation

Liang, J., Lin, L., Yang, M., Wang, J., & Lu, J. (2017). The therapeutic implication of a novel SCN2A mutation associated early-onset epileptic encephalopathy with Rett-like features. Brain & Development, 39(10), 877. https://doi.org/10.1016/j.braindev.2017.06.003

Chicago Style (17th ed.) Citation

Liang, Jao-Shwann, Li-Ju Lin, Ming-Tao Yang, Jinn-Shyan Wang, and Jyh-Feng Lu. "The Therapeutic Implication of a Novel SCN2A Mutation Associated Early-onset Epileptic Encephalopathy with Rett-like Features." Brain & Development 39, no. 10 (2017): 877. https://doi.org/10.1016/j.braindev.2017.06.003.

MLA (9th ed.) Citation

Liang, Jao-Shwann, et al. "The Therapeutic Implication of a Novel SCN2A Mutation Associated Early-onset Epileptic Encephalopathy with Rett-like Features." Brain & Development, vol. 39, no. 10, 2017, p. 877, https://doi.org/10.1016/j.braindev.2017.06.003.