Clinical Phenotype and Outcome of Hypertrophic Cardiomyopathy Associated With Thin-Filament Gene Mutations

BACKGROUND: Mild hypertrophy but increased arrhythmic risk characterizes the stereotypic phenotype proposed for hypertrophic cardiomyopathy (HCM) caused by thin-filament mutations. However, whether such clinical profile is different from more prevalent thick-filament–associated disease is unresolved...

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Detalles Bibliográficos
Autores principales: Coppini, Raffaele, Ho, Carolyn Y., Ashley, Euan, Day, Sharlene, Ferrantini, Cecilia, Girolami, Francesca, Tomberli, Benedetta, Bardi, Sara, Torricelli, Francesca, Cecchi, Franco, Mugelli, Alessandro, Poggesi, Corrado, Tardiff, Jil, Olivotto, Iacopo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Biomedical 2014
Materias:
Original Investigation
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4270453/
https://www.ncbi.nlm.nih.gov/pubmed/25524337
http://dx.doi.org/10.1016/j.jacc.2014.09.059

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4270453/
https://www.ncbi.nlm.nih.gov/pubmed/25524337
http://dx.doi.org/10.1016/j.jacc.2014.09.059

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