Exploring digenic inheritance in arrhythmogenic cardiomyopathy

BACKGROUND: Arrhythmogenic cardiomyopathy (ACM) is an inherited genetic disorder, characterized by the substitution of heart muscle with fibro-fatty tissue and severe ventricular arrhythmias, often leading to heart failure and sudden cardiac death. ACM is considered a monogenic disorder, but the low...

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Detalles Bibliográficos
Autores principales: König, Eva, Volpato, Claudia Béu, Motta, Benedetta Maria, Blankenburg, Hagen, Picard, Anne, Pramstaller, Peter, Casella, Michela, Rauhe, Werner, Pompilio, Giulio, Meraviglia, Viviana, Domingues, Francisco S., Sommariva, Elena, Rossini, Alessandra
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5723071/
https://www.ncbi.nlm.nih.gov/pubmed/29221435
http://dx.doi.org/10.1186/s12881-017-0503-7

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5723071/
https://www.ncbi.nlm.nih.gov/pubmed/29221435
http://dx.doi.org/10.1186/s12881-017-0503-7

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