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...

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Detalles Bibliográficos
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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Article
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

Internet

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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