CCDC39 is required for assembly of inner dynein arms and the dynein regulatory complex and for normal ciliary motility in humans and dogs.
(65/140)
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The coiled-coil domain containing protein CCDC40 is essential for motile cilia function and left-right axis formation.
(66/140)
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Population specificity of the DNAI1 gene mutation spectrum in primary ciliary dyskinesia (PCD).
(67/140)
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Ciliopathies: an expanding disease spectrum.
(68/140)
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TTC21B contributes both causal and modifying alleles across the ciliopathy spectrum.
(69/140)
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Nasal nitric oxide and nitric oxide synthase expression in primary ciliary dyskinesia.
(70/140)
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Torque teno virus viremia load size in patients with selected congenital defects of innate immunity.
(71/140)
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Inner dynein arm defects causing primary ciliary dyskinesia: repeat testing required.
(72/140)
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