A rare case of arrhythmogenic right ventricular cardiomyopathy associated with LAMA2 mutation: A case report and literature review

BACKGROUND: Arrhythmogenic right ventricular cardiomyopathy (ARVC) is a heritable heart muscle disorder that predominantly affects the right ventricle. Mutations in genes that encode components of desmosomes, the adhesive junctions that connect cardiomyocytes, are the predominant cause of ARVC. A ca...

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Detalles Bibliográficos
Autores principales: Wang, Yue, Fang, Yibing, Zhang, Dan, Li, Yifei, Luo, Shuhua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Medicine
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9339636/
https://www.ncbi.nlm.nih.gov/pubmed/35924034
http://dx.doi.org/10.3389/fmed.2022.922347

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9339636/
https://www.ncbi.nlm.nih.gov/pubmed/35924034
http://dx.doi.org/10.3389/fmed.2022.922347

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