Referenced in: none

Automatically associated channels: Nav1.5

Title: A homozygous SCN5A mutation in a severe, recessive type of cardiac conduction disease.

Authors: Axel Neu, Michele Eiselt, Matthias Paul, Kathrin Sauter, Birgit Stallmeyer, Dirk Isbrandt, Eric Schulze-Bahr

Journal, date & volume: Hum. Mutat., 2010 Aug , 31, E1609-21

PubMed link: http://www.ncbi.nlm.nih.gov/pubmed/20564468

Abstract