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

Internet

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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