Atypical endocrine manifestations in Gordon syndrome caused by CUL3 mutation: a case report.

Fatahichegeni M, Ansarian MA, Lv H, Fu J

Open source

DOI: 10.3389/fmed.2026.1862901
Published: 2026
Container: Frontiers in medicine
Publisher: Not recorded
Open access: yes

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Cite this work

BibTeX

@article{allodium:10.3389/fmed.2026.1862901,
  title = {Atypical endocrine manifestations in Gordon syndrome caused by CUL3 mutation: a case report.},
  author = {Fatahichegeni M and Ansarian MA and Lv H and Fu J},
  year = {2026},
  journal = {Frontiers in medicine},
  doi = {10.3389/fmed.2026.1862901},
  url = {https://doi.org/10.3389/fmed.2026.1862901}
}

RIS

TY  - JOUR
TI  - Atypical endocrine manifestations in Gordon syndrome caused by CUL3 mutation: a case report.
AU  - Fatahichegeni M
AU  - Ansarian MA
AU  - Lv H
AU  - Fu J
PY  - 2026
JO  - Frontiers in medicine
DO  - 10.3389/fmed.2026.1862901
UR  - https://doi.org/10.3389/fmed.2026.1862901
ER  -

APA

M, F., MA, A., H, L., & J, F. (2026). Atypical endocrine manifestations in Gordon syndrome caused by CUL3 mutation: a case report.. Frontiers in medicine. https://doi.org/10.3389/fmed.2026.1862901

Source records

pubmed · retrieved 2026-09-26T17:56:30.908Z
europe-pmc · retrieved 2026-09-26T17:56:30.924Z
doaj · retrieved 2026-09-26T17:56:30.910Z