APA (7th ed.) Citation

JJ, S., Q, C., M, X., YN, L., WR, L., J, L., . . . F, Z. (2022). Loss of Protein Function Causing Severe Phenotypes of Female-Restricted Wieacker Wolff Syndrome due to a Novel Nonsense Mutation in the ZC4H2 Gene. Genes, 13(9), . https://doi.org/10.3390/genes13091558

Chicago Style (17th ed.) Citation

JJ, Sun, et al. "Loss of Protein Function Causing Severe Phenotypes of Female-Restricted Wieacker Wolff Syndrome Due to a Novel Nonsense Mutation in the ZC4H2 Gene." Genes 13, no. 9 (2022). https://doi.org/10.3390/genes13091558.

MLA (9th ed.) Citation

JJ, Sun, et al. "Loss of Protein Function Causing Severe Phenotypes of Female-Restricted Wieacker Wolff Syndrome Due to a Novel Nonsense Mutation in the ZC4H2 Gene." Genes, vol. 13, no. 9, 2022, https://doi.org/10.3390/genes13091558.