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Repression of ferritin light chain translation by human eIF3
A central problem in human biology remains the discovery of causal molecular links between mutations identified in genome-wide association studies (GWAS) and their corresponding disease traits. This challenge is magnified for variants residing in non-coding regions of the genome. Single-nucleotide p...
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| Опубликовано в: : | eLife |
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| Главные авторы: | , , , , , , |
| Формат: | Artigo |
| Язык: | Inglês |
| Опубликовано: |
eLife Sciences Publications, Ltd
2019
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| Предметы: | |
| Online-ссылка: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6721798/ https://ncbi.nlm.nih.gov/pubmed/31414986 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.7554/eLife.48193 |
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