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Cell Type-Specific Annotation and Fine Mapping of Variants Associated With Brain Disorders
Common genetic variants confer susceptibility to a large number of complex brain disorders. Given that such variants predominantly localize in non-coding regions of the human genome, there is a significant challenge to predict and characterize their functional consequences. More importantly, most av...
Tallennettuna:
| Julkaisussa: | Front Genet |
|---|---|
| Päätekijät: | , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
Frontiers Media S.A.
2020
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7744805/ https://ncbi.nlm.nih.gov/pubmed/33343624 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fgene.2020.575928 |
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