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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書誌詳細
出版年:J Am Heart Assoc
主要な著者: 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.
フォーマット: Artigo
言語:Inglês
出版事項: John Wiley and Sons Inc. 2021
主題:
Original Research
オンライン･アクセス: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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