1. Phenotypic variability among patients with hyperornithinaemia–hyperammonaemia–homocitrullinuria syndrome homozygous for the delF188 mutation in SLC25A15. Issue 11 (31st October 2008) Authors: Debray, F-G; Lambert, M; Lemieux, B; Soucy, J F; Drouin, R; Fenyves, D; Dubé, J; Maranda, B; Laframboise, R; Mitchell, G A Journal: Journal of medical genetics Issue: Volume 45:Issue 11(2008) Page Start: 759 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗