PubMed 23376825
Referenced in: none
Automatically associated channels: Kv7.1 , Nav1.5
Title: Digenic inheritance novel mutations in SCN5a and SNTA1 increase late I(Na) contributing to LQT syndrome.
Authors: Rou-Mu Hu, Bi-Hua Tan, Kate M Orland, Carmen R Valdivia, Amber Peterson, Jielin Pu, Jonathan C Makielski
Journal, date & volume: Am. J. Physiol. Heart Circ. Physiol., 2013 Apr 1 , 304, H994-H1001
PubMed link: http://www.ncbi.nlm.nih.gov/pubmed/23376825
Abstract