1. Primary carnitine deficiency: novel mutations and insights into the cardiac phenotype. (12th March 2013) Authors: Shibbani, K.; Fahed, A.C.; Al‐Shaar, L.; Arabi, M.; Nemer, G.; Bitar, F.; Majdalani, M. Journal: Clinical genetics Issue: Volume 85:Number 2(2014:Feb.) Page Start: 127 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗