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Paper Details

<i>IFT74</i> variants cause skeletal ciliopathy and motile cilia defects in mice and humans.
medRxiv
0
2023
Humans, IFT subunit, IFT subunits, IFT74, Ift74, cell, ciliary chondrodysplasia, exon 2, exon 2 deletion, human, human and mouse variants, humans, mice, midgestational lethality, motile, motile cilia, motile cilia defects, mouse, mouse allele, mucociliary clearance disorders, primary cilia, skeletal abnormalities, skeletal chondrodysplasia, skeletal ciliopathy, tubulin

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Release 1.2