Article
Examining the Association between Mitochondrial Genome Variation and Coronary Artery Disease
2022-02-10
Abstract excerpt
<h4>Background</h4> Large-scale genome-wide association studies have identified hundreds of single-nucleotide variants (SNVs) significantly associated with coronary artery disease (CAD). However, collectively, these explain <20% of the heritability. <h4>Hypothesis</h4> Here, we hypothesize that mitochondrial (MT) SNVs might present one potential source of this “missing heritability”. <h4>Methods</h4> We analyzed 2...
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Identifiers and source
- Literature Corpus work
- 1e1d5c6b-6e7b-5532-80e7-688cf0587ae6
- DOI
- 10.1101/2022.02.09.22270723
