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New Variant in Placophilin-2 Gene Causing Arrhythmogenic Myocardiopathy
Introduction: Arrhythmogenic cardiomyopathy (ACM) is an inherited disease characterized by progressive fibroadipose replacement of cardiomyocytes. Its diagnosis is based on imaging, electrocardiographic, histological and genetic/familial criteria. The development of the disease is based mainly on de...
Autores principales: | Caimi-Martinez, Fiama, Antoniutti, Guido, Blanco, Rocio, García de la Villa, Bernardo, Alvarenga, Nelson, Govea-Callizo, Nancy, Torres-Juan, Laura, Heine-Suñer, Damián, Rosell-Andreo, Jordi, Luengos, David Crémer, Alvarez-Rubio, Jorge, Ripoll-Vera, Tomás |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9141741/ https://www.ncbi.nlm.nih.gov/pubmed/35627167 http://dx.doi.org/10.3390/genes13050782 |
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