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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| Principais autores: | , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Wiley
2019-12-01
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| Colecção: | Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease |
| Assuntos: | |
| Acesso em linha: | https://www.ahajournals.org/doi/10.1161/JAHA.119.012993 |
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