Phenotypic Expression and Outcomes in Individuals With Rare Genetic Variants of Hypertrophic Cardiomyopathy

BACKGROUND: Hypertrophic cardiomyopathy (HCM) is caused by rare variants in sarcomere-encoding genes, but little is known about the clinical significance of these variants in the general population. OBJECTIVES: The goal of this study was to compare lifetime outcomes and cardiovascular phenotypes acc...

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Detalles Bibliográficos
Autores principales: de Marvao, Antonio, McGurk, Kathryn A., Zheng, Sean L., Thanaj, Marjola, Bai, Wenjia, Duan, Jinming, Biffi, Carlo, Mazzarotto, Francesco, Statton, Ben, Dawes, Timothy J.W., Savioli, Nicolò, Halliday, Brian P., Xu, Xiao, Buchan, Rachel J., Baksi, A. John, Quinlan, Marina, Tokarczuk, Paweł, Tayal, Upasana, Francis, Catherine, Whiffin, Nicola, Theotokis, Pantazis I., Zhang, Xiaolei, Jang, Mikyung, Berry, Alaine, Pantazis, Antonis, Barton, Paul J.R., Rueckert, Daniel, Prasad, Sanjay K., Walsh, Roddy, Ho, Carolyn Y., Cook, Stuart A., Ware, James S., O’Regan, Declan P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Biomedical 2021
Materias:
Original Investigation
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8434420/
https://www.ncbi.nlm.nih.gov/pubmed/34503678
http://dx.doi.org/10.1016/j.jacc.2021.07.017

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8434420/
https://www.ncbi.nlm.nih.gov/pubmed/34503678
http://dx.doi.org/10.1016/j.jacc.2021.07.017

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