Assessing the Role of Rare Genetic Variation in Patients With Heart Failure

IMPORTANCE: Sequencing studies have identified causal genetic variants for distinct subtypes of heart failure (HF) such as hypertrophic or dilated cardiomyopathy. However, the role of rare, high-impact variants in HF, for which ischemic heart disease is the leading cause, has not been systematically...

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Detalhes bibliográficos
Publicado no:JAMA Cardiol
Main Authors: Povysil, Gundula, Chazara, Olympe, Carss, Keren J., Deevi, Sri V. V., Wang, Quanli, Armisen, Javier, Paul, Dirk S., Granger, Christopher B., Kjekshus, John, Aggarwal, Vimla, Haefliger, Carolina, Goldstein, David B.
Formato: Artigo
Idioma:Inglês
Publicado em: American Medical Association 2020
Assuntos:
Original Investigation
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC7745141/
https://ncbi.nlm.nih.gov/pubmed/33326012
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1001/jamacardio.2020.6500
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