Genetic Causes of Cardiomyopathy in Children: First Results From the Pediatric Cardiomyopathy Genes Study

BACKGROUND: Pediatric cardiomyopathy is a genetically heterogeneous disease with substantial morbidity and mortality. Current guidelines recommend genetic testing in children with hypertrophic, dilated, or restrictive cardiomyopathy, but practice variations exist. Robust data on clinical testing pra...

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Detalles Bibliográficos
Autores principales: Ware, Stephanie M., Wilkinson, James D., Tariq, Muhammad, Schubert, Jeffrey A., Sridhar, Arthi, Colan, Steven D., Shi, Ling, Canter, Charles E., Hsu, Daphne T., Webber, Steven A., Dodd, Debra A., Everitt, Melanie D., Kantor, Paul F., Addonizio, Linda J., Jefferies, John L., Rossano, Joseph W., Pahl, Elfriede, Rusconi, Paolo, Chung, Wendy K., Lee, Teresa, Towbin, Jeffrey A., Lal, Ashwin K., Bhatnagar, Surbhi, Aronow, Bruce, Dexheimer, Phillip J., Martin, Lisa J., Miller, Erin M., Sleeper, Lynn A., Razoky, Hiedy, Czachor, Jason, Lipshultz, Steven E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Original Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8200745/
https://www.ncbi.nlm.nih.gov/pubmed/33906374
http://dx.doi.org/10.1161/JAHA.120.017731

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8200745/
https://www.ncbi.nlm.nih.gov/pubmed/33906374
http://dx.doi.org/10.1161/JAHA.120.017731

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