1. Longitudinal phenotypic study of late-onset retinal degeneration due to a founder variant c.562C>A p.(Pro188Thr) in the C1QTNF5 gene. (3rd September 2021) Authors: De Zaeytijd, Julie; Coppieters, Frauke; De Bruyne, Marieke; Van Royen, Jasper; Roels, Dimitri; Six, Rani; Van Cauwenbergh, Caroline; De Baere, Elfride; Leroy, Bart P. Journal: Ophthalmic genetics Issue: Volume 42:Number 5(2021) Page Start: 521 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗