Genetic modulation of brugada syndrome by a common polymorphism.
Lizotte E, Junttila MJ, Dube MP, Hong K, Benito B, DE Zutter M, Henkens S, Sarkozy A, Huikuri HV, Towbin J, Vatta M, Brugada P, Brugada J, Brugada R.
Lizotte E, et al. Among authors: brugada r, brugada p, brugada j.
J Cardiovasc Electrophysiol. 2009 Oct;20(10):1137-41. doi: 10.1111/j.1540-8167.2009.01508.x. Epub 2009 Jun 22.
J Cardiovasc Electrophysiol. 2009.
PMID: 19549036
We studied whether common variant H558R has any clinical implications in the phenotype of Brugada syndrome. METHODS: Our study population consisted of Brugada syndrome subjects 75 with SCN5A mutation and 92 without SCN5A mutation. ...RESULTS: The AA genotype carrier …
We studied whether common variant H558R has any clinical implications in the phenotype of Brugada syndrome. METHODS: Our study popula …