Genetic determinants of clinical phenotype in hypertrophic cardiomyopathy

BACKGROUND: Hypertrophic cardiomyopathy (HCM) is the most common inherited cardiovascular disease that affects approximately one in 500 people. HCM is a recognized genetic disorder most often caused by mutations involving myosin-binding protein C (MYBPC3) and β-myosin heavy chain (MYH7) which are re...

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Bibliographic Details
Published in:BMC Cardiovasc Disord
Main Authors: Velicki, Lazar, Jakovljevic, Djordje G., Preveden, Andrej, Golubovic, Miodrag, Bjelobrk, Marija, Ilic, Aleksandra, Stojsic, Snezana, Barlocco, Fausto, Tafelmeier, Maria, Okwose, Nduka, Tesic, Milorad, Brennan, Paul, Popovic, Dejana, Ristic, Arsen, MacGowan, Guy A., Filipovic, Nenad, Maier, Lars S., Olivotto, Iacopo
Format: Artigo
Language:Inglês
Published: BioMed Central 2020
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Research Article
Online Access:https://ncbi.nlm.nih.gov/pmc/articles/PMC7727200/
https://ncbi.nlm.nih.gov/pubmed/33297970
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12872-020-01807-4
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