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Whole genome sequence analysis of blood lipid levels in >66,000 individuals
Blood lipids are heritable modifiable causal factors for coronary artery disease. Despite well-described monogenic and polygenic bases of dyslipidemia, limitations remain in discovery of lipid-associated alleles using whole genome sequencing (WGS), partly due to limited sample sizes, ancestral diver...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9553944/ https://www.ncbi.nlm.nih.gov/pubmed/36220816 http://dx.doi.org/10.1038/s41467-022-33510-7 |