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Phenotypic clustering of dilated cardiomyopathy patients highlights important pathophysiological differences

AIMS: The dilated cardiomyopathy (DCM) phenotype is the result of combined genetic and acquired triggers. Until now, clinical decision-making in DCM has mainly been based on ejection fraction (EF) and NYHA classification, not considering the DCM heterogenicity. The present study aimed to identify pa...

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Detalles Bibliográficos
Autores principales:	Verdonschot, Job A J, Merlo, Marco, Dominguez, Fernando, Wang, Ping, Henkens, Michiel T H M, Adriaens, Michiel E, Hazebroek, Mark R, Masè, Marco, Escobar, Luis E, Cobas-Paz, Rafael, Derks, Kasper W J, van den Wijngaard, Arthur, Krapels, Ingrid P C, Brunner, Han G, Sinagra, Gianfranco, Garcia-Pavia, Pablo, Heymans, Stephane R B
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Oxford University Press 2020
Materias:	Clinical Research
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7813623/ https://www.ncbi.nlm.nih.gov/pubmed/33156912 http://dx.doi.org/10.1093/eurheartj/ehaa841

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