An international compendium of mutations in the SCN5A-encoded cardiac sodium channel in patients referred for Brugada syndrome genetic testing

BACKGROUND: Brugada syndrome (BrS) is a common heritable channelopathy. Mutations in the SCN5A-encoded sodium channel (BrS1) culminate in the most common genotype. OBJECTIVE: This study sought to perform a retrospective analysis of BrS databases from 9 centers that have each genotyped >100 unrela...

ver descrição completa

Na minha lista:
Detalhes bibliográficos
Main Authors: Kapplinger, Jamie D., Tester, David J., Alders, Marielle, Benito, Begoña, Berthet, Myriam, Brugada, Josep, Brugada, Pedro, Fressart, Véronique, Guerchicoff, Alejandra, Harris-Kerr, Carole, Kamakura, Shiro, Kyndt, Florence, Koopmann, Tamara T., Miyamoto, Yoshihiro, Pfeiffer, Ryan, Pollevick, Guido D., Probst, Vincent, Zumhagen, Sven, Vatta, Matteo, Towbin, Jeffrey A., Shimizu, Wataru, Schulze-Bahr, Eric, Antzelevitch, Charles, Salisbury, Benjamin A., Guicheney, Pascale, Wilde, Arthur A. M., Brugada, Ramon, Schott, Jean-Jacques, Ackerman, Michael J.
Formato: Artigo
Idioma:Inglês
Publicado em: 2009
Assuntos:
Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2822446/
https://ncbi.nlm.nih.gov/pubmed/20129283
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.hrthm.2009.09.069
Tags: Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!

Registos relacionados