Familial glucocorticoid deficiency due to a novel TXNRD2 variant: expanding the spectrum of a rare genetic cause.
- DOI
- 10.3389/fendo.2026.1834727
- Published
- 2026
- Container
- Frontiers in endocrinology
- Publisher
- Not recorded
- Open access
- yes
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Cite this work
BibTeX
@article{allodium:10.3389/fendo.2026.1834727,
title = {Familial glucocorticoid deficiency due to a novel TXNRD2 variant: expanding the spectrum of a rare genetic cause.},
author = {Al Alwan I and Alhamoudi KM and Alzaben AI and Almulhem B and Qawasmi N and Alswailem M and Alotaibi S and Alsaihati B and Jabaan A and Mahzari M and Flück CE and Alzahrani AS},
year = {2026},
journal = {Frontiers in endocrinology},
doi = {10.3389/fendo.2026.1834727},
url = {https://doi.org/10.3389/fendo.2026.1834727}
}RIS
TY - JOUR TI - Familial glucocorticoid deficiency due to a novel TXNRD2 variant: expanding the spectrum of a rare genetic cause. AU - Al Alwan I AU - Alhamoudi KM AU - Alzaben AI AU - Almulhem B AU - Qawasmi N AU - Alswailem M AU - Alotaibi S AU - Alsaihati B AU - Jabaan A AU - Mahzari M AU - Flück CE AU - Alzahrani AS PY - 2026 JO - Frontiers in endocrinology DO - 10.3389/fendo.2026.1834727 UR - https://doi.org/10.3389/fendo.2026.1834727 ER -
APA
I, A. A., KM, A., AI, A., B, A., N, Q., M, A., S, A., B, A., A, J., M, M., CE, F., & AS, A. (2026). Familial glucocorticoid deficiency due to a novel TXNRD2 variant: expanding the spectrum of a rare genetic cause.. Frontiers in endocrinology. https://doi.org/10.3389/fendo.2026.1834727
Source records
- pubmed · retrieved 2026-09-26T21:01:43.068Z
- europe-pmc · retrieved 2026-09-26T21:01:43.087Z
- doaj · retrieved 2026-09-26T21:01:43.084Z