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Article

Cilia, primary ciliary dyskinesia and molecular genetics.

Paediatric respiratory reviews - 1 Mar 2004

Chodhari R, Mitchison H M, Meeks M

Abstract excerpt

Primary ciliary dyskinesia (PCD) is a phenotypically and genetically heterogeneous condition in which three genetic mutations have already been identified. The primary defect is in the ultrastructure or function of cilia, highly complex organelles that are structurally related to the flagella of sperm and protozoa. The clinical features of PCD include recurrent sinopulmonary infections, subfertility and...

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Identifiers

PMID: 15222957
DOI: 10.1016/j.prrv.2003.09.005

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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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