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Article

Rare hypertension as a result of 17alpha-hydroxylase deficiency.

Journal of pediatric endocrinology & metabolism : JPEM - 1 Jan 2011

Wang Wei, Fu Jun-Fen, Gong Fang-Qi, Zhu Wei-Hua, Shen Zheng

Abstract excerpt

PURPOSE: To investigate CYP 7A1 gene mutations in Chinese patients with 17alpha-hydroxylase deficiency. METHODS: Clinical data were retrospectively analyzed. CYP17A1 mutations were detected in two cases with 17alpha-hydroxylase deficiency. Genomic DNA was isolated from blood samples and eight primers pairs were used to amplify eight exons and exon-intron boundaries of the CYP17A1 gene. The amplified PCR products...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 21823532
DOI: 10.1515/jpem.2011.008

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

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