IFT74 variants cause skeletal ciliopathy and motile cilia defects in mice and humans.
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PLoS Genet. 2023 Jun 14;19(6):e1010796. doi: 10.1371/journal.pgen.1010796. eCollection 2023 Jun.
PLoS Genet. 2023.
PMID: 37315079
Free PMC article.