Referenced in: none

Automatically associated channels: Nav1.5

Title: Genetic variants in SCN5A promoter are associated with arrhythmia phenotype severity in patients with heterozygous loss-of-function mutation.

Authors: Ji Kwon Park, Lisa J Martin, Xue Zhang, Anil G Jegga, D Woodrow Benson

Journal, date & volume: Heart Rhythm, 2012 Jul , 9, 1090-6

PubMed link: http://www.ncbi.nlm.nih.gov/pubmed/22370247

Abstract