Penetrance of Hypertrophic Cardiomyopathy in Sarcomere Protein Mutation Carriers

BACKGROUND: Predictive genetic screening of relatives of patients with hypertrophic cardiomyopathy (HCM) caused by sarcomere protein (SP) gene mutations is current standard of care, but there are few data on long-term outcomes in mutation carriers without HCM. OBJECTIVES: The aim of this study was t...

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Detalles Bibliográficos
Autores principales: Lorenzini, Massimiliano, Norrish, Gabrielle, Field, Ella, Ochoa, Juan Pablo, Cicerchia, Marcos, Akhtar, Mohammed M., Syrris, Petros, Lopes, Luis R., Kaski, Juan Pablo, Elliott, Perry M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Biomedical 2020
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7397507/
https://www.ncbi.nlm.nih.gov/pubmed/32731933
http://dx.doi.org/10.1016/j.jacc.2020.06.011

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7397507/
https://www.ncbi.nlm.nih.gov/pubmed/32731933
http://dx.doi.org/10.1016/j.jacc.2020.06.011

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