Genetic Variant Burden and Adverse Outcomes in Pediatric Cardiomyopathy

BACKGROUND: Previous genetic research in pediatric cardiomyopathy (CM) has focused on pathogenic variants for diagnostic purposes, with limited data evaluating genotype-outcome correlations. We explored whether greater genetic variant burden (pathogenic or variants of unknown significance, VUS) corr...

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Publicado en:Pediatr Res
Autores principales: Burstein, Danielle S., Gaynor, J. William, Griffis, Heather, Ritter, Alyssa, O’Connor, Matthew J., Rossano, Joseph W., Lin, Kimberly Y., Ahrens-Nicklas, Rebecca C.
Formato: Artigo
Lenguaje:Inglês
Publicado: 2020
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Article
Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC8256333/
https://ncbi.nlm.nih.gov/pubmed/32746448
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41390-020-1101-5
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