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 genot...

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Autors principals:	Jaap I. van Waning, Joost Moesker, Daphne Heijsman, Eric Boersma, Danielle Majoor‐Krakauer
Format:	Artigo
Idioma:	Inglês
Publicat:	Wiley 2019-12-01
Col·lecció:	Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease
Matèries:	diagnostics genetics human left ventricular noncompaction noncompaction cardiomyopathy outcome
Accés en línia:	https://www.ahajournals.org/doi/10.1161/JAHA.119.012993
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