Article
Genetic Determinants of Clinical Phenotype in Hypertrophic Cardiomyopathy
2020-12-11
Abstract excerpt
<title>Abstract</title> <p><bold>Background:</bold> 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 responsible for approximately three-quarters of the identified mutations.<bold...
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Identifiers and source
- Literature Corpus work
- a5505e33-52ac-5fcc-8cce-ae33cf7c46e0
- DOI
- 10.21203/rs.3.rs-36810/v5
