Case report: Clinical characteristics and Genetical analysis of HSD11B2 in three Chinese children with apparent mineralocorticoid excess: a case series.

Ding Y, Cheng M, Cao B, Liu M, Hu X, Wu D

DOI: 10.3389/fendo.2024.1491825
Published: 2024
Container: Frontiers in endocrinology
Publisher: Not recorded
Open access: yes

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Cite this work

BibTeX

@article{allodium:10.3389/fendo.2024.1491825,
  title = {Case report: Clinical characteristics and Genetical analysis of HSD11B2 in three Chinese children with apparent mineralocorticoid excess: a case series.},
  author = {Ding Y and Cheng M and Cao B and Liu M and Hu X and Wu D},
  year = {2024},
  journal = {Frontiers in endocrinology},
  doi = {10.3389/fendo.2024.1491825},
  url = {https://doi.org/10.3389/fendo.2024.1491825}
}

RIS

TY  - JOUR
TI  - Case report: Clinical characteristics and Genetical analysis of HSD11B2 in three Chinese children with apparent mineralocorticoid excess: a case series.
AU  - Ding Y
AU  - Cheng M
AU  - Cao B
AU  - Liu M
AU  - Hu X
AU  - Wu D
PY  - 2024
JO  - Frontiers in endocrinology
DO  - 10.3389/fendo.2024.1491825
UR  - https://doi.org/10.3389/fendo.2024.1491825
ER  -

APA

Y, D., M, C., B, C., M, L., X, H., & D, W. (2024). Case report: Clinical characteristics and Genetical analysis of HSD11B2 in three Chinese children with apparent mineralocorticoid excess: a case series.. Frontiers in endocrinology. https://doi.org/10.3389/fendo.2024.1491825

Source records

pubmed · retrieved 2026-09-25T20:05:51.732Z