Severe congenital nephrogenic diabetes insipidus in a compound heterozygote with a new large deletion of the AQP2 gene. A case report.
- DOI
- 10.1002/mgg3.568
- Published
- 2019-02-19
- Container
- Mol Genet Genomic Med
- Publisher
- Not recorded
- Open access
- yes
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Cite this work
BibTeX
@article{allodium:10.1002/mgg3.568,
title = {Severe congenital nephrogenic diabetes insipidus in a compound heterozygote with a new large deletion of the AQP2 gene. A case report.},
author = {Peces R and Mena R and Peces C and Santos-Simarro F and Fernández L and Afonso S and Lapunzina P and Selgas R and Nevado J.},
year = {2019},
journal = {Mol Genet Genomic Med},
doi = {10.1002/mgg3.568},
url = {https://doi.org/10.1002/mgg3.568}
}RIS
TY - JOUR TI - Severe congenital nephrogenic diabetes insipidus in a compound heterozygote with a new large deletion of the AQP2 gene. A case report. AU - Peces R AU - Mena R AU - Peces C AU - Santos-Simarro F AU - Fernández L AU - Afonso S AU - Lapunzina P AU - Selgas R AU - Nevado J. PY - 2019 JO - Mol Genet Genomic Med DO - 10.1002/mgg3.568 UR - https://doi.org/10.1002/mgg3.568 ER -
APA
R, P., R, M., C, P., F, S., L, F., S, A., P, L., R, S., & J., N. (2019). Severe congenital nephrogenic diabetes insipidus in a compound heterozygote with a new large deletion of the AQP2 gene. A case report.. Mol Genet Genomic Med. https://doi.org/10.1002/mgg3.568
Source records
- europe-pmc · retrieved 2026-09-27T15:23:43.094Z