1. A mutation creating an out‐of‐frame alternative translation initiation site in the GRHPR 5′UTR causing primary hyperoxaluria type II. (26th December 2014) Authors: Fu, Y.; Rope, R.; Fargue, S.; Cohen, H.T.; Holmes, R.P.; Cohen, D.M. Journal: Clinical genetics Issue: Volume 88:Number 5(2015:Nov.) Page Start: 494 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗