Genetic determinants of clinical phenotype in hypertrophic cardiomyopathy

Genetic determinants of clinical phenotype in hypertrophic cardiomyopathy

Abstract 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) whic...

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Main Authors: Lazar Velicki, Djordje G. Jakovljevic, Andrej Preveden, Miodrag Golubovic, Marija Bjelobrk, Aleksandra Ilic, Snezana Stojsic, Fausto Barlocco, Maria Tafelmeier, Nduka Okwose, Milorad Tesic, Paul Brennan, Dejana Popovic, Arsen Ristic, Guy A. MacGowan, Nenad Filipovic, Lars S. Maier, Iacopo Olivotto
Format: Article
Language:English
Published: BMC 2020-12-01
Series:BMC Cardiovascular Disorders
Subjects:
Hypertrophic cardiomyopathy
HCM
Hereditary cardiac disease
Left ventricular hypertrophy
MYBPC3
MYH7
Online Access:https://doi.org/10.1186/s12872-020-01807-4

Internet

https://doi.org/10.1186/s12872-020-01807-4

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