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...

Description complète

Enregistré dans:
Détails bibliographiques
Publié dans:Pediatr Res
Auteurs principaux: Burstein, Danielle S., Gaynor, J. William, Griffis, Heather, Ritter, Alyssa, O’Connor, Matthew J., Rossano, Joseph W., Lin, Kimberly Y., Ahrens-Nicklas, Rebecca C.
Format: Artigo
Langue:Inglês
Publié: 2020
Sujets:
Article
Accès en ligne: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
Tags: Ajouter un tag
Pas de tags, Soyez le premier à ajouter un tag!

Documents similaires