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Article

Heterogeneous spectrum of CFTR gene mutations in Chinese patients with CAVD and the dilemma of genetic blocking strategy.

Reproduction (Cambridge, England) - 1 Sept 2022

Feng Jiarong, Zhang Yanan, Yang Xiaojian, Zhang Yan

Abstract excerpt

In brief: The genetic heterogeneity of CFTR gene mutations in Chinese patients with congenital absence of the vas deferens (CAVD) differs from the hotspot mutation pattern in Caucasians. This paper reviews and suggests a more suitable screening strategy for the Chinese considering the dilemma of CFTR genetic blocking. Abstract: Congenital absence of the vas deferens (CAVD) is a major cause of obstructive...

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Identifiers

PMID: 35913788
DOI: 10.1530/REP-21-0315

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

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