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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Detalles Bibliográficos
Autores principales: 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: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7727200/
https://www.ncbi.nlm.nih.gov/pubmed/33297970
http://dx.doi.org/10.1186/s12872-020-01807-4

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7727200/
https://www.ncbi.nlm.nih.gov/pubmed/33297970
http://dx.doi.org/10.1186/s12872-020-01807-4

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