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.
Zang L, Gong Y, Li Y, Dou J, Lyu Z, Su X, Zhang Y, Mu Y. Biomed Res Int. 2022; 2022:7073158. Epub 2022 Jul 12.