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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 no: | Pediatr Res |
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| Main Authors: | , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2020
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| Assuntos: | |
| Acesso em linha: | 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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