Cite
A Novel Missense Mutation of Arginine Vasopressin Receptor 2 in a Chinese Family with Congenital Nephrogenic Diabetes Insipidus: X-Chromosome Inactivation in Female CNDI Patients with Heterozygote 814A>G Mutation.
MLA
Zang, Li, et al. “A Novel Missense Mutation of Arginine Vasopressin Receptor 2 in a Chinese Family with Congenital Nephrogenic Diabetes Insipidus: X-Chromosome Inactivation in Female CNDI Patients with Heterozygote 814A>G Mutation.” BioMed Research International, July 2022, pp. 1–7. EBSCOhost, https://doi.org/10.1155/2022/7073158.
APA
Zang, L., Gong, Y., Li, Y., Dou, J., Lyu, Z., Su, X., Zhang, Y., & Mu, Y. (2022). A Novel Missense Mutation of Arginine Vasopressin Receptor 2 in a Chinese Family with Congenital Nephrogenic Diabetes Insipidus: X-Chromosome Inactivation in Female CNDI Patients with Heterozygote 814A>G Mutation. BioMed Research International, 1–7. https://doi.org/10.1155/2022/7073158
Chicago
Zang, Li, Yuping Gong, Yijun Li, Jingtao Dou, Zhaohui Lyu, Xiaoqing Su, Yawei Zhang, and Yiming Mu. 2022. “A Novel Missense Mutation of Arginine Vasopressin Receptor 2 in a Chinese Family with Congenital Nephrogenic Diabetes Insipidus: X-Chromosome Inactivation in Female CNDI Patients with Heterozygote 814A>G Mutation.” BioMed Research International, July, 1–7. doi:10.1155/2022/7073158.