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Paper Details

TTC21B contributes both causal and modifying alleles across the ciliopathy spectrum.
Nat Genet
272
2011
Ciliary dysfunction, TTC21B, causal genes, ciliopathies, ciliopathy, disease-causing genes, inherited, inherited disorders, isolated nephronophthisis, retrograde intraflagellar transport protein IFT139, syndromic Jeune asphyxiating thoracic dystrophy

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Release 1.2