Familial Hypomagnesemia With Hypercalciuria and Nephrocalcinosis: A Case Report of Compound Heterozygous Variants in the CLDN16 Gene Inherited From Symptomatic Heterozygous Carriers.
- DOI
- 10.1159/cnd/abxag006
- Published
- 2026 Jan-Dec
- Container
- Case reports in nephrology and dialysis
- Publisher
- Not recorded
- Open access
- yes
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Cite this work
BibTeX
@article{allodium:10.1159/cnd/abxag006,
title = {Familial Hypomagnesemia With Hypercalciuria and Nephrocalcinosis: A Case Report of Compound Heterozygous Variants in the CLDN16 Gene Inherited From Symptomatic Heterozygous Carriers.},
author = {Ceol M and Sgrò E and Anglani F and Priante G and Stefanelli LF and Cacciapuoti M and Salviati L and Nalesso F and Del Prete D},
year = {2026},
journal = {Case reports in nephrology and dialysis},
doi = {10.1159/cnd/abxag006},
url = {https://doi.org/10.1159/cnd/abxag006}
}RIS
TY - JOUR TI - Familial Hypomagnesemia With Hypercalciuria and Nephrocalcinosis: A Case Report of Compound Heterozygous Variants in the CLDN16 Gene Inherited From Symptomatic Heterozygous Carriers. AU - Ceol M AU - Sgrò E AU - Anglani F AU - Priante G AU - Stefanelli LF AU - Cacciapuoti M AU - Salviati L AU - Nalesso F AU - Del Prete D PY - 2026 JO - Case reports in nephrology and dialysis DO - 10.1159/cnd/abxag006 UR - https://doi.org/10.1159/cnd/abxag006 ER -
APA
M, C., E, S., F, A., G, P., LF, S., M, C., L, S., F, N., & D, D. P. (2026). Familial Hypomagnesemia With Hypercalciuria and Nephrocalcinosis: A Case Report of Compound Heterozygous Variants in the CLDN16 Gene Inherited From Symptomatic Heterozygous Carriers.. Case reports in nephrology and dialysis. https://doi.org/10.1159/cnd/abxag006
Source records
- pubmed · retrieved 2026-11-10T10:49:49.734Z
- europe-pmc · retrieved 2026-11-10T10:49:49.733Z