A NOVEL MUTATION IN THE HCN4 GENE CAUSES SYMPTOMATIC SINUS BRADYCARDIA IN MOROCCAN JEWS

OBJECTIVES: To conduct a clinical, genetic and functional analysis of three unrelated families with familial sinus bradycardia (FSB). BACKGROUND: Mutations in the hyperpolarization-activated nucleotide-gated channel (HCN4) are known to be associated with FSB. METHODS AND RESULTS: Three males of Moro...

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Detalhes bibliográficos
Main Authors: Laish-Farkash, Avishag, Brass, Dovrat, Marek-Yagel, Dina, Pras, Elon, Dascal, Nathan, Antzelevitch, Charles, Nof, Eyal, Reznik, Haya, Eldar, Michael, Glikson, Michael, Luria, David
Formato: Artigo
Idioma:Inglês
Publicado em: 2010
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3005590/
https://ncbi.nlm.nih.gov/pubmed/20662977
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/j.1540-8167.2010.01844.x
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