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C deletion of the SLC39A8 gene polymorphism (rs74650330) increases the risk of coronary artery disease in individuals with low LDL cholesterol levels

2020-08-04

Abstract excerpt

<title>Abstract</title> <p><bold>Background:</bold> The genetic variant of <italic>SLC39A8</italic> is associated with several cardiovascular disease risk factors, including body mass index, systolic blood pressure (SBP), diastolic blood pressure (DBP), N-terminal pro-B-type natriuretic peptide (NT-proBNP) and high-density lipoprotein cholesterol (HDL-C) levels. The present study aimed to investigate the associat...

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Literature Corpus work
a1510568-0b4d-5792-b99f-47d93539df76
DOI
10.21203/rs.3.rs-51681/v1
Open publication

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C deletion of the SLC39A8 gene polymorphism (rs74650330) increases the risk of coronary artery disease in individuals with low LDL cholesterol levelsDOI 10.21203/rs.3.rs-51681/v1
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