1. A common SCN5A polymorphism attenuates a severe cardiac phenotype caused by a nonsense SCN5A mutation in a Chinese family with an inherited cardiac conduction defect. Issue 10 (17th May 2006) Authors: Niu, Dau-Ming; Hwang, Betau; Hwang, Han-Wei; Wang, Nana H; Wu, Jer-Yuarn; Lee, Pi-Chang; Chien, Jen-Chung; Shieh, Ru-Chi; Chen, Yuan-Tsong Journal: Journal of medical genetics Issue: Volume 43:Issue 10(2006) Page Start: 817 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗