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Examining the Association between Mitochondrial Genome Variation and Coronary Artery Disease

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. Hypothesis: Here, we hypothesize that mitochondrial (MT)-SNVs might...

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Detalles Bibliográficos
Autores principales:	Vilne, Baiba, Sawant, Aniket, Rudaka, Irina
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	MDPI 2022
Materias:	Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8953999/ https://www.ncbi.nlm.nih.gov/pubmed/35328073 http://dx.doi.org/10.3390/genes13030516

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