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Article

Genetic mutation analysis of 22 patients with congenital absence of vas deferens: a single-center study†.

Biology of reproduction - 13 Jan 2022

Tan Mao-Qing, Huang Wu-Jian, Lan Feng-Hua, Xu Yong-Jun, Zheng Mei-Yu, Tang Ying

Abstract excerpt

Congenital absence of the vas deferens (CAVD), a congenital malformation of the male reproductive system, causes obstructive azoospermia and male infertility. Currently, the cystic fibrosis transmembrane conductance regulator (CFTR) has been recognized as the main pathogenic gene in CAVD, with some other genes, such as adhesion G-protein-coupled receptor G2 (ADGRG2), solute carrier family 9 isoform 3 (SLC9A3),...

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Identifiers

PMID: 34673937
DOI: 10.1093/biolre/ioab194

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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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