1. A substitution mutation in cardiac ubiquitin ligase, FBXO32, is associated with an autosomal recessive form of dilated cardiomyopathy. Issue 1 (December 2016) Authors: Al-Hassnan, Zuhair; Shinwari, Zarghuna; Wakil, Salma; Tulbah, Sahar; Mohammed, Shamayel; Rahbeeni, Zuhair; Alghamdi, Mohammed; Rababh, Monther; Colak, Dilek; Kaya, Namik; Al-Fayyadh, Majid; Alburaiki, Jehad Journal: BMC medical genetics Issue: Volume 17:Issue 1(2016) Page Start: 1 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗