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.
Li ZangYuping GongYijun LiJingtao DouZhaohui LyuXiaoqing SuYawei ZhangYi-Ming MuPublished in: BioMed research international (2022)
gene.