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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...
Shranjeno v:
| izdano v: | BMC Med Genet |
|---|---|
| Main Authors: | , , , , , , , , , , , , |
| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
BioMed Central
2017
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| Teme: | |
| Online dostop: | 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 |
| Oznake: |
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