Genetic analysis of Brugada syndrome and congenital long-QT syndrome type 3 in the Chinese

BACKGROUND: Brugada syndrome and congenital long-QT syndrome (LQTS) type 3 (LQT3) are 2 inherited conditions of abnormal cardiac excitability characterized clinically by an increased risk of ventricular tachyarrhythmias. SCN5A gene that encodes the cardiac sodium channel α subunit is responsible for...

Descripción completa

Detalles Bibliográficos
Autores principales: Liang, Peng, Liu, Wenling, Li, Cuilan, Tao, Wuhua, Li, Lei, Hu, Dayi
Formato: Texto
Lenguaje:English
Publicado: Medknow Publications 2010
Materias:
Original Paper
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2945207/
https://www.ncbi.nlm.nih.gov/pubmed/20877689
http://dx.doi.org/10.4103/0975-3583.64437

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2945207/
https://www.ncbi.nlm.nih.gov/pubmed/20877689
http://dx.doi.org/10.4103/0975-3583.64437

Ejemplares similares