1. IFT80 mutations cause a novel complex ciliopathy phenotype with retinal degeneration. Issue 3 (17th July 2018) Authors: Moran, J.; G. Sanderson, K.; Maynes, J.; Vig, A.; Batmanabane, V.; Kannu, P.; Tavares, E.; Vincent, A.; Héon, E. Journal: Clinical genetics Issue: Volume 94:Issue 3/4(2018) Page Start: 368 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗