Rare types of congenital adrenal hyperplasia: report of five children with 11β-hydroxylase deficiency including pathogenic and novel CYP11B1 variants
- DOI
- 10.20945/2359-4292-2026-0073
- Published
- 2026
- Container
- Archives of Endocrinology and Metabolism
- Publisher
- Archives of Endocrinology and Metabolism
- Open access
- unknown
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Cite this work
BibTeX
@article{allodium:10.20945/2359-4292-2026-0073,
title = {Rare types of congenital adrenal hyperplasia: report of five children with 11β-hydroxylase deficiency including pathogenic and novel CYP11B1 variants},
author = {Anju Bala and Sayan Banerjee and Arun George and Priyanka Srivastava and Mohit Kumar and Neha KC and Jaivinder Yadav and Rakesh Kumar and Devi Dayal},
year = {2026},
journal = {Archives of Endocrinology and Metabolism},
doi = {10.20945/2359-4292-2026-0073},
url = {https://doi.org/10.20945/2359-4292-2026-0073}
}RIS
TY - JOUR TI - Rare types of congenital adrenal hyperplasia: report of five children with 11β-hydroxylase deficiency including pathogenic and novel CYP11B1 variants AU - Anju Bala AU - Sayan Banerjee AU - Arun George AU - Priyanka Srivastava AU - Mohit Kumar AU - Neha KC AU - Jaivinder Yadav AU - Rakesh Kumar AU - Devi Dayal PY - 2026 JO - Archives of Endocrinology and Metabolism DO - 10.20945/2359-4292-2026-0073 UR - https://doi.org/10.20945/2359-4292-2026-0073 ER -
APA
Bala, A., Banerjee, S., George, A., Srivastava, P., Kumar, M., KC, N., Yadav, J., Kumar, R., & Dayal, D. (2026). Rare types of congenital adrenal hyperplasia: report of five children with 11β-hydroxylase deficiency including pathogenic and novel CYP11B1 variants. Archives of Endocrinology and Metabolism. https://doi.org/10.20945/2359-4292-2026-0073
Source records
- crossref · retrieved 2026-09-26T14:12:34.263Z