Order Article Reprints

Sun J-J, Cai Q, Xu M, Liu Y-N, Li W-R, Li J, Ma L, Cai C, Gong X-H, Zeng Y-T, 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. 2022; 13(9):1558. https://doi.org/10.3390/genes13091558

Sun, Jing-Jing, Qin Cai, Miao Xu, Yan-Na Liu, Wan-Rui Li, Juan Li, Li Ma, Cheng Cai, Xiao-Hui Gong, Yi-Tao Zeng, and et al. 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, no. 9: 1558. https://doi.org/10.3390/genes13091558

Sun, J. -J., Cai, Q., Xu, M., Liu, Y. -N., Li, W. -R., Li, J., Ma, L., Cai, C., Gong, X. -H., Zeng, Y. -T., Ren, Z. -R., & Zeng, F. (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), 1558. https://doi.org/10.3390/genes13091558