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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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Literature Corpus work
a5505e33-52ac-5fcc-8cce-ae33cf7c46e0
DOI
10.21203/rs.3.rs-36810/v5
Open publication

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Genetic Determinants of Clinical Phenotype in Hypertrophic CardiomyopathyDOI 10.21203/rs.3.rs-36810/v5
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