Whole genome sequence analysis of blood lipid levels in >66,000 individuals
Although the common genetic variants contributing to blood lipid levels have been studied, the contribution of rare variants is less understood. Here, the authors perform a rare coding and noncoding variant association study of blood lipid levels using whole genome sequencing data.
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| Médium: | Artigo |
| Jazyk: | Inglês |
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Nature Portfolio
2022-10-01
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| Edice: | Nature Communications |
| On-line přístup: | https://doi.org/10.1038/s41467-022-33510-7 |
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