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.
- DOI
- 10.1155/2022/7073158
- Published
- 2022
- Container
- BioMed research international
- Publisher
- Not recorded
- Open access
- yes
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Cite this work
BibTeX
@article{allodium:10.1155/2022/7073158,
title = {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.},
author = {Zang L and Gong Y and Li Y and Dou J and Lyu Z and Su X and Zhang Y and Mu Y},
year = {2022},
journal = {BioMed research international},
doi = {10.1155/2022/7073158},
url = {https://doi.org/10.1155/2022/7073158}
}RIS
TY - JOUR TI - 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. AU - Zang L AU - Gong Y AU - Li Y AU - Dou J AU - Lyu Z AU - Su X AU - Zhang Y AU - Mu Y PY - 2022 JO - BioMed research international DO - 10.1155/2022/7073158 UR - https://doi.org/10.1155/2022/7073158 ER -
APA
L, Z., Y, G., Y, L., J, D., Z, L., X, S., Y, Z., & Y, M. (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. https://doi.org/10.1155/2022/7073158
Source records
- pubmed · retrieved 2026-09-25T03:07:48.562Z