APA (7th ed.) Citation

Martin, R., Splitt, M., Genevieve, D., Aten, E., Collins, A., de Bie, C. I., . . . van Haeringen, A. (2019). De novo variants in CNOT3 cause a variable neurodevelopmental disorder. European journal of human genetics : EJHG, 27(11), 1677-1682. https://doi.org/10.1038/s41431-019-0413-6

Chicago Style (17th ed.) Citation

Martin, R., et al. "De Novo Variants in CNOT3 Cause a Variable Neurodevelopmental Disorder." European Journal of Human Genetics : EJHG 27, no. 11 (2019): 1677-1682. https://doi.org/10.1038/s41431-019-0413-6.

MLA (9th ed.) Citation

Martin, R., et al. "De Novo Variants in CNOT3 Cause a Variable Neurodevelopmental Disorder." European Journal of Human Genetics : EJHG, vol. 27, no. 11, 2019, pp. 1677-1682, https://doi.org/10.1038/s41431-019-0413-6.