Extended genotype-phenotype spectrum of 17α-hydroxylase/17,20-lyase deficiency: a nine-case series featuring a novel mutation, suspected TART-like lesions, and multisystem involvement.

Chong H, Fu Y, Zhang X, Zhang Y, Yan X, Pi Y

Open source

DOI: 10.3389/fendo.2026.1824733
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.2026.1824733,
  title = {Extended genotype-phenotype spectrum of 17α-hydroxylase/17,20-lyase deficiency: a nine-case series featuring a novel mutation, suspected TART-like lesions, and multisystem involvement.},
  author = {Chong H and Fu Y and Zhang X and Zhang Y and Yan X and Pi Y},
  year = {2026},
  journal = {Frontiers in endocrinology},
  doi = {10.3389/fendo.2026.1824733},
  url = {https://doi.org/10.3389/fendo.2026.1824733}
}

RIS

TY  - JOUR
TI  - Extended genotype-phenotype spectrum of 17α-hydroxylase/17,20-lyase deficiency: a nine-case series featuring a novel mutation, suspected TART-like lesions, and multisystem involvement.
AU  - Chong H
AU  - Fu Y
AU  - Zhang X
AU  - Zhang Y
AU  - Yan X
AU  - Pi Y
PY  - 2026
JO  - Frontiers in endocrinology
DO  - 10.3389/fendo.2026.1824733
UR  - https://doi.org/10.3389/fendo.2026.1824733
ER  -

APA

H, C., Y, F., X, Z., Y, Z., X, Y., & Y, P. (2026). Extended genotype-phenotype spectrum of 17α-hydroxylase/17,20-lyase deficiency: a nine-case series featuring a novel mutation, suspected TART-like lesions, and multisystem involvement.. Frontiers in endocrinology. https://doi.org/10.3389/fendo.2026.1824733

Source records

pubmed · retrieved 2026-11-10T11:40:37.213Z
europe-pmc · retrieved 2026-11-10T11:40:37.220Z
doaj · retrieved 2026-11-10T11:40:37.212Z