Prevalence of arrhythmia-associated gene mutations and risk of sudden cardiac death in the Finnish population

BACKGROUND: Sudden cardiac death (SCD) remains a major cause of death in Western Countries. It has a heritable component, but previous molecular studies have mainly focused on common genetic variants. We studied the prevalence, clinical phenotypes, and risk of SCD presented by ten rare mutations pre...

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Detalhes bibliográficos
Main Authors: Lahtinen, Annukka M., Havulinna, Aki S., Noseworthy, Peter A., Jula, Antti, Karhunen, Pekka J., Perola, Markus, Newton-Cheh, Christopher, Salomaa, Veikko, Kontula, Kimmo
Formato: Artigo
Idioma:Inglês
Publicado em: 2013
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3778376/
https://ncbi.nlm.nih.gov/pubmed/23651034
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3109/07853890.2013.783995
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