Center-Authored Papers
Filters: Author is Arts, Heleen H [Clear All Filters]
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2008. CC2D2A is mutated in Joubert syndrome and interacts with the ciliopathy-associated basal body protein CEP290.. American journal of human genetics. 83(5):559-71. Abstract
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2015. The Ciliopathy Protein CC2D2A Associates with NINL and Functions in RAB8-MICAL3-Regulated Vesicle Trafficking.. PLoS genetics. 11(10):e1005575. Abstract
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