# Retracted: 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

**Authors:** BioMed Research International

PMC · DOI: 10.1155/2024/9753837 · BioMed Research International · 2024-03-20

## Full-text entities

- **Genes:** AVPR2 (arginine vasopressin receptor 2) [NCBI Gene 554] {aka ADHR, DI1, DIR, DIR3, NDI, NDI1}
- **Diseases:** Congenital Nephrogenic Diabetes Insipidus (MESH:D018500)
- **Species:** Homo sapiens (human, species) [taxon 9606]
- **Mutations:** 814A>G

## Full text

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## References

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Source: https://tomesphere.com/paper/PMC10977231