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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Библиографические подробности
Главные авторы: Marjamaa, Annukka, Laitinen-Forsblom, Päivi, Lahtinen, Annukka M, Viitasalo, Matti, Toivonen, Lauri, Kontula, Kimmo, Swan, Heikki
Формат: Artigo
Язык:Inglês
Опубликовано: BioMed Central 2009
Предметы:
Research Article
Online-ссылка: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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