Alterations in Calcium Handling Are a Common Feature in an Arrhythmogenic Cardiomyopathy Cell Model Triggered by Desmosome Genes Loss

Arrhythmogenic cardiomyopathy (ACM) is an inherited cardiac disease characterized by fibrofatty replacement of the myocardium. Deleterious variants in desmosomal genes are the main cause of ACM and lead to common and gene-specific molecular alterations, which are not yet fully understood. This artic...

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Detalles Bibliográficos
Autores principales: Vallverdú-Prats, Marta, Carreras, David, Pérez, Guillermo J., Campuzano, Oscar, Brugada, Ramon, Alcalde, Mireia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9917020/
https://www.ncbi.nlm.nih.gov/pubmed/36768439
http://dx.doi.org/10.3390/ijms24032109

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9917020/
https://www.ncbi.nlm.nih.gov/pubmed/36768439
http://dx.doi.org/10.3390/ijms24032109

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