APA (7th ed.) Citation

Webster, R., Cho, M., Retterer, K., Millan, F., Nowak, C., Douglas, J., . . . Chung, W. (2017). De novo loss of function mutations in KIAA2022 are associated with epilepsy and neurodevelopmental delay in females. Clinical Genetics, 91(5), 756. https://doi.org/10.1111/cge.12854

Chicago Style (17th ed.) Citation

Webster, R., et al. "De Novo Loss of Function Mutations in KIAA2022 Are Associated with Epilepsy and Neurodevelopmental Delay in Females." Clinical Genetics 91, no. 5 (2017): 756. https://doi.org/10.1111/cge.12854.

MLA (9th ed.) Citation

Webster, R., et al. "De Novo Loss of Function Mutations in KIAA2022 Are Associated with Epilepsy and Neurodevelopmental Delay in Females." Clinical Genetics, vol. 91, no. 5, 2017, p. 756, https://doi.org/10.1111/cge.12854.