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Article

CCDC40 mutation as a cause of infertility in a Chinese family with primary ciliary dyskinesia.

Medicine - 23 Dec 2021

Liu Li, Zhou Kechong, Song Yuxuan, Liu Xiaoqiang

Abstract excerpt

TRIAL DESIGN: Primary ciliary dyskinesia (PCD) is a genetical disease that inherited in an autosomal-recessive way. Its clinical manifestations (such as male infertility) are mainly caused by defects of motion-related cilia that encoded by mutated genes. Although some mutation has been verified, a number of mutations of PCD remain elusive. The main purpose of this study is to identify mutant genes in a Chinese...

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Identifiers

PMID: 34941110
DOI: 10.1097/MD.0000000000028275
PMCID: PMC8702141

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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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