A combinatorial oligogenic basis for the phenotypic plasticity between late-onset dilated and arrhythmogenic cardiomyopathy in a single family

INTRODUCTION: Primary dilated cardiomyopathy (DCM) and arrhythmogenic right ventricular cardiomyopathy (ARVC) are the two common and distinct forms of hereditary cardiomyopathies caused by defined pathogenic variants (PVs) typically in different sets of genes. DCM is characterized by left ventricula...

Descripción completa

Detalles Bibliográficos
Autores principales: Pourebrahim, Kimia, Marian, John Garrity, Tan, Yanli, Chang, Jeffrey T., Marian, Ali J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8594872/
https://www.ncbi.nlm.nih.gov/pubmed/34790974
http://dx.doi.org/10.20517/jca.2021.15

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8594872/
https://www.ncbi.nlm.nih.gov/pubmed/34790974
http://dx.doi.org/10.20517/jca.2021.15

Ejemplares similares