TTC21B contributes both causal and modifying alleles across the ciliopathy spectrum

22 publications in the local catalog that cite this work (OpenAlex reference match; not the full global list).

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2. 2015 Joubert syndrome a model for untangling recessive disorders with extreme genetic heterogeneityCitations 298 · OpenAlex
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10. 2013 Exome sequencing identifies DYNC2H1 mutations as a common cause of asphyxiating thoracic dystrophy Jeune syndrome without major polydactyly renal or retinal involvementCitations 146 · OpenAlex