Referenced in: none

Automatically associated channels: Kir2.3 , Nav1.5

Title: Compound heterozygosity for mutations (W156X and R225W) in SCN5A associated with severe cardiac conduction disturbances and degenerative changes in the conduction system.

Authors: Connie R Bezzina, Martin B Rook, W Antoinette Groenewegen, Lucas J Herfst, Allard C van der Wal, Jan Lam, Habo J Jongsma, Arthur A M Wilde, Marcel M A M Mannens

Journal, date & volume: Circ. Res., 2003 Feb 7 , 92, 159-68

PubMed link: http://www.ncbi.nlm.nih.gov/pubmed/12574143

Abstract