Case Report: Compound heterozygous mutation comprising p.Pro31Leu and exons 1–3 ins/del variants in CYP21A2 causes non-classical congenital adrenal hyperplasia in a Chinese girl

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Journal
Frontiers in Pediatrics
Published
2026-03-31
DOI
https://doi.org/10.3389/fped.2026.1778805
Primary Topic
Sexual Differentiation and Disorders
Type
article
Field-Weighted Citation Impact
0.00

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article

Case Report: Compound heterozygous mutation comprising p.Pro31Leu and exons 1–3 ins/del variants in CYP21A2 causes non-classical congenital adrenal hyperplasia in a Chinese girl

Harvest F. Gu, Chao Lu, Xiaofei An, Nan Li
Frontiers in Pediatrics
Sexual Differentiation and Disorders
article

Case Report: Compound heterozygous mutation comprising p.Pro31Leu and exons 1–3 ins/del variants in CYP21A2 causes non-classical congenital adrenal hyperplasia in a Chinese girl

Harvest F. Gu, Chao Lu, Xiaofei An, Nan Li
article en

Abstract

No abstract available for this paper.
Frontiers in PediatricsVol. 14
Nanjing University of Chinese Medicine (CN), Qilu University of Technology (CN), China Pharmaceutical University (CN)
Government of Jiangsu Province
Good health and well-being
Openalex Percentile: Top 31%
Sexual Differentiation and Disorders
DOIOpen Access PDFOpenAlex
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