IgA nephropathy in a patient with 17α-hydroxylase/17,20-lyase deficiency caused by the CYP17A1 p. Y329fs mutation: a case report and review
- DOI
- 10.1186/s12887-026-07487-x
- Published
- 2026-08-06
- Container
- BMC Pediatrics
- Publisher
- Springer Science and Business Media LLC
- Open access
- unknown
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Cite this work
BibTeX
@article{allodium:10.1186/s12887-026-07487-x,
title = {IgA nephropathy in a patient with 17α-hydroxylase/17,20-lyase deficiency caused by the CYP17A1 p. Y329fs mutation: a case report and review},
author = {Ying Guo and Hong Jian Xie and Wei Dai and Ting Liu},
year = {2026},
journal = {BMC Pediatrics},
doi = {10.1186/s12887-026-07487-x},
url = {https://doi.org/10.1186/s12887-026-07487-x}
}RIS
TY - JOUR TI - IgA nephropathy in a patient with 17α-hydroxylase/17,20-lyase deficiency caused by the CYP17A1 p. Y329fs mutation: a case report and review AU - Ying Guo AU - Hong Jian Xie AU - Wei Dai AU - Ting Liu PY - 2026 JO - BMC Pediatrics DO - 10.1186/s12887-026-07487-x UR - https://doi.org/10.1186/s12887-026-07487-x ER -
APA
Guo, Y., Xie, H. J., Dai, W., & Liu, T. (2026). IgA nephropathy in a patient with 17α-hydroxylase/17,20-lyase deficiency caused by the CYP17A1 p. Y329fs mutation: a case report and review. BMC Pediatrics. https://doi.org/10.1186/s12887-026-07487-x
Source records
- crossref · retrieved 2026-11-07T08:03:24.636Z