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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Bibliografiska uppgifter
I publikationen:BMC Med Genet
Huvudupphovsmän: 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
Materialtyp: Artigo
Språk:Inglês
Publicerad: BioMed Central 2017
Ämnen:
Research Article
Länkar:https://ncbi.nlm.nih.gov/pmc/articles/PMC5723071/
https://ncbi.nlm.nih.gov/pubmed/29221435
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12881-017-0503-7
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