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Missing heritability of common diseases and treatments outside the protein-coding exome
Genetic factors strongly influence risk of common human diseases and treatment outcomes but the causative variants remain largely unknown; this gap has been called the ‘missing heritability’. We propose several hypotheses that in combination have the potential to narrow the gap. First, given a multi...
Tallennettuna:
| Päätekijät: | , , , , , |
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| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
2014
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4169001/ https://ncbi.nlm.nih.gov/pubmed/25107510 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00439-014-1476-7 |
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