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

Internet

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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