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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Detalhes bibliográficos
Publicado no: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
Formato: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2020
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Research Article
Acesso em linha: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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