Life-long tailoring of management for patients with hypertrophic cardiomyopathy: Awareness and decision-making in changing scenarios

Hypertrophic cardiomyopathy (HCM) is the most common genetic heart disease, characterised by complex pathophysiology and extensive genetic and clinical heterogeneity. In most patients, HCM is caused by mutations in cardiac sarcomere protein genes and inherited as an autosomal dominant trait. The cli...

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Detalles Bibliográficos
Autores principales: Michels, M., Olivotto, I., Asselbergs, F. W., van der Velden, J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Bohn Stafleu van Loghum 2016
Materias:
Original Article – Point of View
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5313451/
https://www.ncbi.nlm.nih.gov/pubmed/28005231
http://dx.doi.org/10.1007/s12471-016-0943-2

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5313451/
https://www.ncbi.nlm.nih.gov/pubmed/28005231
http://dx.doi.org/10.1007/s12471-016-0943-2

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