APA (7th ed.) Citation

J, C., A, R., K, C., E, B., P, S., A, G., . . . G, N. (2022). uORF-introducing variants in the 5'UTR of the NIPBL gene as a cause of Cornelia de Lange syndrome. Human mutation, 43(9), 1239. https://doi.org/10.1002/humu.24384

Chicago Style (17th ed.) Citation

J, Coursimault, et al. "UORF-introducing Variants in the 5'UTR of the NIPBL Gene as a Cause of Cornelia De Lange Syndrome." Human Mutation 43, no. 9 (2022): 1239. https://doi.org/10.1002/humu.24384.

MLA (9th ed.) Citation

J, Coursimault, et al. "UORF-introducing Variants in the 5'UTR of the NIPBL Gene as a Cause of Cornelia De Lange Syndrome." Human Mutation, vol. 43, no. 9, 2022, p. 1239, https://doi.org/10.1002/humu.24384.