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...

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Detalles Bibliográficos
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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Mini‐Review
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

Internet

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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