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Article

The role of the F508C mutation in congenital bilateral absence of the vas deferens.

Genetics in medicine : official journal of the American College of Medical Genetics - 1 Dec 2008

Havasi Viktoria, Keiles Steven, Hambuch Tina, Sorscher Eric J, Kammesheidt Anja

Abstract excerpt

PURPOSE: Congenital bilateral absence of the vas deferens is a pathologic condition associated with normal spermatogenesis, azoospermia, and lack of both vasa deferentia. A significant association between mutations in the cystic fibrosis transmembrane conductance regulator gene among men with con...

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Source

Identifiers

PMID: 19092444
DOI: 10.1097/GIM.0b013e31818e594d

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-19092444-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

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

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