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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Dades bibliogràfiques
Publicat a:J Am Heart Assoc
Autors principals: 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.
Format: Artigo
Idioma:Inglês
Publicat: John Wiley and Sons Inc. 2021
Matèries:
Original Research
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC8200745/
https://ncbi.nlm.nih.gov/pubmed/33906374
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1161/JAHA.120.017731
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