RetractedArticleBioMed research international2022

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 Zang et al.PubMed ↗Full text ↗Publisher ↗

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