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Article

Studies of a co-chaperone of the androgen receptor, FKBP52, as candidate for hypospadias.

Reproductive biology and endocrinology : RB&E - 7 Mar 2007

Beleza-Meireles Ana, Barbaro Michela, Wedell Anna, Töhönen Virpi, Nordenskjöld Agneta

Abstract excerpt

BACKGROUND: Hypospadias is a common inborn error of the male urethral development, for which the aetiology is still elusive. Polymorphic variants in genes involved in the masculinisation of male genitalia, such as the androgen receptor, have been associated with some cases of hypospadias. Co-regulators of the androgen receptor start being acknowledged as possible candidates for hormone-resistance instances, which...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Share to Polymorphism, Single Nucleotide

Share to Receptors, Androgen

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Source

Open in PubMed Open full text

Identifiers

PMID: 17343741
DOI: 10.1186/1477-7827-5-8
PMCID: PMC1821330

Genes

FKBP4

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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Studies of a co-chaperone of the androgen receptor, FKBP52, as candidate for hypospadias.PMID 17343741Read ↗

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