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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...
Autores principales: | Wang, Yue, Fang, Yibing, Zhang, Dan, Li, Yifei, Luo, Shuhua |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
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 |
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