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

Por Niu, Dau‐Ming, Hwang, Betau, Hwang, Han‐Wei, Wang, Nana H, Wu, Jer‐Yuarn, Lee, Pi‐Chang, Chien, Jen‐Chung, Shieh, Ru‐Chi
Publicado em 2006