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Article

[Molecular basis of cystic fibrosis and congenital bilateral agenesis of vas deferens].

Contraception, fertilite, sexualite (1992) - 1 Jun 1996

Bienvenu T, Claustres M

Abstract excerpt

Cystic fibrosis (CF) is the most common severe autosomal recessive disorder of the Caucasian population. Since the identification of the CFTR (Cystic Fibrosis Transmembrane Conductance Regulator) gene in 1989, over 550 mutations have been characterized. CFTR can function as a chloride channel wit...

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Source

Identifiers

PMID: 8766513

Genes

CFTR

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 1 Sept 2026. Prepared record publication-8766513-2026-09-01.1. Manifest publication-graph-cohort-2026-09-01.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 1 Sept 2026.

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[Molecular basis of cystic fibrosis and congenital bilateral agenesis of vas deferens].PMID 8766513Read ↗

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Mutations of the cystic fibrosis transmembrane conductance regulator gene in males with congenital bilateral absence of the vas deferens: Reproductive implications and genetic counseling (Review).Semantic proximity Read ↗

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[Detection of pathogenic gene mutations in thirteen cases of congenital bilateral absence of vas deferens infertility patients].Semantic proximity Read ↗

Mutations in the cystic fibrosis gene in patients with congenital absence of the vas deferens.Semantic proximity Read ↗

[Gene mutations in congenital bilateral absence of the vas deferens: An update].Semantic proximity Read ↗

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