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Dark matter RNA illuminates the puzzle of genome-wide association studies
In the past decade, numerous studies have made connections between sequence variants in human genomes and predisposition to complex diseases. However, most of these variants lie outside of the charted regions of the human genome whose function we understand; that is, the sequences that encode protei...
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| Autors principals: | , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
BioMed Central
2014
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4054906/ https://ncbi.nlm.nih.gov/pubmed/24924000 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1741-7015-12-97 |
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