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Pediatric Hypertrophic Cardiomyopathy: Exploring the Genotype‐Phenotype Association
Pediatric hypertrophic cardiomyopathy (HCM) is the most common form of cardiomyopathy in children and a leading cause of sudden cardiac death. Yet, the association between genotype variation, phenotype expression, and adverse events in pediatric HCM has not been fully elucidated. Although the litera...
Autores principales: | Nguyen, Minh B., Mital, Seema, Mertens, Luc, Jeewa, Aamir, Friedberg, Mark K., Aguet, Julien, Adler, Arnon, Lam, Christopher Z., Dragulescu, Andreea, Rakowski, Harry, Villemain, Olivier |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9075072/ https://www.ncbi.nlm.nih.gov/pubmed/35179047 http://dx.doi.org/10.1161/JAHA.121.024220 |
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