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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...

Täydet tiedot

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Bibliografiset tiedot
Päätekijät: St. Laurent, Georges, Vyatkin, Yuri, Kapranov, Philipp
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: BioMed Central 2014
Aiheet:
Linkit: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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