SGK3 promoter deletion in late-onset hypophosphatemic rickets, a possible genetic cause of the disease.
- DOI
- 10.1186/s13023-026-04335-0
- Published
- 2026 Mar 30
- Container
- Orphanet journal of rare diseases
- Publisher
- Not recorded
- Open access
- yes
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limited evidence Score 45/100 under policy 1.0.0. This is a metadata assessment, not a judgment of the paper's conclusions.
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Cite this work
BibTeX
@article{allodium:10.1186/s13023-026-04335-0,
title = {SGK3 promoter deletion in late-onset hypophosphatemic rickets, a possible genetic cause of the disease.},
author = {Uçar A and Albader N and Qattan A and BinEssa HA and Özdemir EM and Özdemir M and Zou M and Alzahrani AS and Shi Y},
year = {2026},
journal = {Orphanet journal of rare diseases},
doi = {10.1186/s13023-026-04335-0},
url = {https://doi.org/10.1186/s13023-026-04335-0}
}RIS
TY - JOUR TI - SGK3 promoter deletion in late-onset hypophosphatemic rickets, a possible genetic cause of the disease. AU - Uçar A AU - Albader N AU - Qattan A AU - BinEssa HA AU - Özdemir EM AU - Özdemir M AU - Zou M AU - Alzahrani AS AU - Shi Y PY - 2026 JO - Orphanet journal of rare diseases DO - 10.1186/s13023-026-04335-0 UR - https://doi.org/10.1186/s13023-026-04335-0 ER -
APA
A, U., N, A., A, Q., HA, B., EM, Ö., M, Ö., M, Z., AS, A., & Y, S. (2026). SGK3 promoter deletion in late-onset hypophosphatemic rickets, a possible genetic cause of the disease.. Orphanet journal of rare diseases. https://doi.org/10.1186/s13023-026-04335-0
Source records
- pubmed · retrieved 2026-09-26T06:32:21.682Z