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Article

An overview of CFTR mutation profiles and assisted reproductive technology outcomes in Chinese patients with congenital obstructive azoospermia.

Journal of assisted reproduction and genetics - 1 Feb 2024

Wang Meng, Zhou Juepu, Long Rui, Mao Ruolin, Gao Limin, Wang Xiangfei, Chen Yinwei, Jin Lei, Zhu Lixia

Abstract excerpt

PURPOSE: The cystic fibrosis transmembrane conductance regulator (CFTR) is the most common causative gene attributed to congenital obstructive azoospermia (OA). The aim of this study was to conduct an epidemiological survey of congenital OA patients, to screen for CFTR mutations, and to follow their pregnancy outcomes in assisted reproductive technology (ART). METHODS: This cohort study enrolled congenital OA...

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Identifiers

PMID: 38114870
DOI: 10.1007/s10815-023-03004-6
PMCID: PMC10894795

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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