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...

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Detalhes bibliográficos
Main Authors: Marjamaa, Annukka, Laitinen-Forsblom, Päivi, Lahtinen, Annukka M, Viitasalo, Matti, Toivonen, Lauri, Kontula, Kimmo, Swan, Heikki
Formato: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2009
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2667497/
https://ncbi.nlm.nih.gov/pubmed/19216760
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2350-10-12
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