Effect of Occurrence of Lamin A/C (LMNA) Genetic Variants in a Cohort of 101 Consecutive Apparent “Lone AF” Patients: Results and Insights

OBJECTIVE: Mutations in the Lamin A/C (LMNA) gene are commonly associated with cardiac manifestations, such as dilated cardiomyopathy (DCM) and conduction system disease. However, the overall spectrum and penetrance of rare LMNA variants are unknown. The present study described the presence of LMNA...

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Detalles Bibliográficos
Autores principales: Pessente, Gabrielle D'Arezzo, Sacilotto, Luciana, Calil, Zaine Oliveira, Olivetti, Natalia Quintella Sangiorgi, Wulkan, Fanny, de Oliveira, Théo Gremen Mimary, Pedrosa, Anísio Alexandre Andrade, Wu, Tan Chen, Hachul, Denise Tessariol, Scanavacca, Maurício Ibrahim, Krieger, José Eduardo, Darrieux, Francisco Carlos da Costa, Pereira, Alexandre da Costa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Cardiovascular Medicine
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9016147/
https://www.ncbi.nlm.nih.gov/pubmed/35449878
http://dx.doi.org/10.3389/fcvm.2022.823717

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9016147/
https://www.ncbi.nlm.nih.gov/pubmed/35449878
http://dx.doi.org/10.3389/fcvm.2022.823717

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