Further Insights in the Most Common SCN5A Mutation Causing Overlapping Phenotype of Long QT Syndrome, Brugada Syndrome, and Conduction Defect
Veltmann, Christian, Barajas‐Martinez, Hector, Wolpert, Christian, Borggrefe, Martin, Schimpf, Rainer, Pfeiffer, Ryan, Cáceres, Gabriel, Burashnikov, Elena, Antzelevitch, Charles, Hu, DanVolume:
5
Language:
english
Journal:
Journal of the American Heart Association
DOI:
10.1161/JAHA.116.003379
Date:
July, 2016
File:
PDF, 2.85 MB
english, 2016