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Article

Mutation analysis of the CYP21A2 gene in the Iranian population.

Genetic testing and molecular biomarkers - 1 Feb 2012

Rabbani Bahareh, Mahdieh Nejat, Ashtiani Mohammad Tahgi Haghi, Larijani Bagher, Akbari Mohammad Taghi, New Maria, Parsa Alan, Schouten Jan P, Rabbani Ali

Abstract excerpt

BACKGROUND: Defects in the CYP21A2 gene cause steroid 21-hydroxylase deficiency, which is the most frequent cause of congenital adrenal hyperplasia. Forty four affected families were investigated to identify the mutation spectrum of the CYP21A2 gene. METHODS: Families were subjected to clinical,...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

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Identifiers

PMID: 22017335
DOI: 10.1089/gtmb.2011.0099
PMCID: PMC3277924

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-22017335-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

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