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Systematic Review of Genotype‐Phenotype Correlations in Noncompaction Cardiomyopathy

BACKGROUND: A genetic cause can be identified in 30% of noncompaction cardiomyopathy patients (NCCM) with clinical features ranging from asymptomatic cardiomyopathy to heart failure with major adverse cardiac events (MACE). METHODS AND RESULTS: To investigate genotype‐phenotype correlations, the gen...

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Detalles Bibliográficos
Autores principales:	van Waning, Jaap I., Moesker, Joost, Heijsman, Daphne, Boersma, Eric, Majoor‐Krakauer, Danielle
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	John Wiley and Sons Inc. 2019
Materias:	Systematic Review and Meta‐analysis
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6912966/ https://www.ncbi.nlm.nih.gov/pubmed/31771441 http://dx.doi.org/10.1161/JAHA.119.012993

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