Search for cardiac calcium cycling gene mutations in familial ventricular arrhythmias resembling catecholaminergic polymorphic ventricular tachycardia

BACKGROUND: Catecholaminergic polymorphic ventricular tachycardia (CPVT) is a severe inherited cardiac disorder caused by mutations predominantly in the ryanodine receptor (RyR2) gene. We sought to identify mutations in genes affecting cardiac calcium cycling in patients with CPVT and in less typica...

Descripción completa

Detalles Bibliográficos
Autores principales: Marjamaa, Annukka, Laitinen-Forsblom, Päivi, Lahtinen, Annukka M, Viitasalo, Matti, Toivonen, Lauri, Kontula, Kimmo, Swan, Heikki
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2667497/
https://www.ncbi.nlm.nih.gov/pubmed/19216760
http://dx.doi.org/10.1186/1471-2350-10-12

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2667497/
https://www.ncbi.nlm.nih.gov/pubmed/19216760
http://dx.doi.org/10.1186/1471-2350-10-12

Ejemplares similares