Evidence-Based Assessment of Genes in Dilated Cardiomyopathy

Each of the cardiomyopathies, classically categorized as hypertrophic cardiomyopathy, dilated cardiomyopathy (DCM), and arrhythmogenic right ventricular cardiomyopathy, has a signature genetic theme. Hypertrophic cardiomyopathy and arrhythmogenic right ventricular cardiomyopathy are largely understo...

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Detalles Bibliográficos
Autores principales: Jordan, Elizabeth, Peterson, Laiken, Ai, Tomohiko, Asatryan, Babken, Bronicki, Lucas, Brown, Emily, Celeghin, Rudy, Edwards, Matthew, Fan, Judy, Ingles, Jodie, James, Cynthia A., Jarinova, Olga, Johnson, Renee, Judge, Daniel P., Lahrouchi, Najim, Lekanne Deprez, Ronald H., Lumbers, R. Thomas, Mazzarotto, Francesco, Medeiros Domingo, Argelia, Miller, Rebecca L., Morales, Ana, Murray, Brittney, Peters, Stacey, Pilichou, Kalliopi, Protonotarios, Alexandros, Semsarian, Christopher, Shah, Palak, Syrris, Petros, Thaxton, Courtney, van Tintelen, J. Peter, Walsh, Roddy, Wang, Jessica, Ware, James, Hershberger, Ray E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2021
Materias:
Original Research Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8247549/
https://www.ncbi.nlm.nih.gov/pubmed/33947203
http://dx.doi.org/10.1161/CIRCULATIONAHA.120.053033

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8247549/
https://www.ncbi.nlm.nih.gov/pubmed/33947203
http://dx.doi.org/10.1161/CIRCULATIONAHA.120.053033

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