1. Variability in clinical phenotypes of PRPF8-linked autosomal dominant retinitis pigmentosa correlates with differential PRPF8/SNRNP200 interactions. (2nd January 2018) Authors: Escher, Pascal; Passarin, Olga; Munier, Francis L.; Tran, Viet H.; Vaclavik, Veronika Journal: Ophthalmic genetics Issue: Volume 39:Number 1(2018) Page Start: 80 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗