Referenced in: none

Automatically associated channels: Kv7.1 , Nav1.5

Title: 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.

Authors: Dau-Ming Niu, Betau Hwang, Han-Wei Hwang, Nana H Wang, Jer-Yuarn Wu, Pi-Chang Lee, Jen-Chung Chien, Ru-Chi Shieh, Yuan-Tsong Chen

Journal, date & volume: J. Med. Genet., 2006 Oct , 43, 817-21

PubMed link: http://www.ncbi.nlm.nih.gov/pubmed/16707561

Abstract