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Genome-wide association and Mendelian randomization study of blood copper levels and 213 deep phenotypes in humans
A genome-wide association study in a Chinese population identifies SNPs associated with serum copper levels. Mendelian randomization analysis reveals causal effects on multiple human phenotypes in East Asian and European populations.
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Main Authors: | , , , , , , , , , , , |
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Formato: | Artigo |
Idioma: | Inglês |
Publicado em: |
Nature Portfolio
2022-05-01
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Colecção: | Communications Biology |
Acesso em linha: | https://doi.org/10.1038/s42003-022-03351-7 |
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