1. A case of hereditary coproporphyria with posterior reversible encephalopathy and novel coproporphyrinogen oxidase gene mutation c.863T>G (p.Leu288Trp). (September 2018) Authors: Lambie, Deborah; Florkowski, Chris; Sies, Chris; Raizis, Anthony; Siu, Wai-Kwan; Towns, Cindy Journal: Annals of clinical biochemistry Issue: Volume 55:Number 5(2018:Sep.) Page Start: 616 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗