Unraveling the Genotype‐Phenotype Relationship in Hypertrophic Cardiomyopathy: Obesity‐Related Cardiac Defects as a Major Disease Modifier

Hypertrophic cardiomyopathy (HCM) is the most common inherited cardiomyopathy and is characterized by asymmetric septal thickening and diastolic dysfunction. More than 1500 mutations in genes encoding sarcomere proteins are associated with HCM. However, the genotype‐phenotype relationship in HCM is...

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Detalles Bibliográficos
Autores principales: Nollet, Edgar E., Westenbrink, B. Daan, de Boer, Rudolf A., Kuster, Diederik W. D., van der Velden, Jolanda
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Contemporary Reviews
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7763714/
https://www.ncbi.nlm.nih.gov/pubmed/33174505
http://dx.doi.org/10.1161/JAHA.120.018641

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7763714/
https://www.ncbi.nlm.nih.gov/pubmed/33174505
http://dx.doi.org/10.1161/JAHA.120.018641

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