1. Genotype–phenotype variability of retinal manifestation in primary hyperoxaluria type 1. (4th March 2018) Authors: Dulz, S.; Bigdon, E.; Atiskova, Y.; Schuettauf, F.; Cerkauskiene, R.; Oh, J.; Brinkert, F. Journal: Ophthalmic genetics Issue: Volume 39:Number 2(2018) Page Start: 275 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗