APA (7th ed.) Citation

O'Donnell-Luria, A. H., & Syrbe, S. (2019). Heterozygous variants in KMT2E cause a spectrum of neurodevelopmental disorders and epilepsy. The American journal of human genetics, 104(6), . https://doi.org/10.1016/j.ajhg.2019.03.021

Chicago Style (17th ed.) Citation

O'Donnell-Luria, Anne H., and Steffen Syrbe. "Heterozygous Variants in KMT2E Cause a Spectrum of Neurodevelopmental Disorders and Epilepsy." The American Journal of Human Genetics 104, no. 6 (2019). https://doi.org/10.1016/j.ajhg.2019.03.021.

MLA (9th ed.) Citation

O'Donnell-Luria, Anne H., and Steffen Syrbe. "Heterozygous Variants in KMT2E Cause a Spectrum of Neurodevelopmental Disorders and Epilepsy." The American Journal of Human Genetics, vol. 104, no. 6, 2019, https://doi.org/10.1016/j.ajhg.2019.03.021.