Familial hypomagnesemia with hypercalciuria and nephrocalcinosis (FHHNC) with ocular involvement due to a novel CLDN19 variant.

Alhothali W, Hijazi S, Alharbi E, Al Fakeeh K, Al Qahtani AT, Almannai M, Al Tuwaijri A, Eyaid W, Alfreihi S

Open source

DOI
10.1080/13816810.2026.2720672
Published
2026 Aug 24
Container
Ophthalmic genetics
Publisher
Not recorded
Open access
unknown

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BibTeX

@article{allodium:10.1080/13816810.2026.2720672,
  title = {Familial hypomagnesemia with hypercalciuria and nephrocalcinosis (FHHNC) with ocular involvement due to a novel CLDN19 variant.},
  author = {Alhothali W and Hijazi S and Alharbi E and Al Fakeeh K and Al Qahtani AT and Almannai M and Al Tuwaijri A and Eyaid W and Alfreihi S},
  year = {2026},
  journal = {Ophthalmic genetics},
  doi = {10.1080/13816810.2026.2720672},
  url = {https://doi.org/10.1080/13816810.2026.2720672}
}

RIS

TY  - JOUR
TI  - Familial hypomagnesemia with hypercalciuria and nephrocalcinosis (FHHNC) with ocular involvement due to a novel CLDN19 variant.
AU  - Alhothali W
AU  - Hijazi S
AU  - Alharbi E
AU  - Al Fakeeh K
AU  - Al Qahtani AT
AU  - Almannai M
AU  - Al Tuwaijri A
AU  - Eyaid W
AU  - Alfreihi S
PY  - 2026
JO  - Ophthalmic genetics
DO  - 10.1080/13816810.2026.2720672
UR  - https://doi.org/10.1080/13816810.2026.2720672
ER  - 

APA

W, A., S, H., E, A., K, A. F., AT, A. Q., M, A., A, A. T., W, E., & S, A. (2026). Familial hypomagnesemia with hypercalciuria and nephrocalcinosis (FHHNC) with ocular involvement due to a novel CLDN19 variant.. Ophthalmic genetics. https://doi.org/10.1080/13816810.2026.2720672

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