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Identification of common genetic variants controlling transcript isoform variation in human whole blood

An understanding of the genetic variation underlying transcript splicing is essential to dissect the molecular mechanisms of common disease. The available evidence from splicing quantitative trait locus (sQTL) studies has been limited to small samples. We performed genome-wide screening to identify...

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Pubblicato in:Nat Genet
Autori principali: Zhang, Xiaoling, Joehanes, Roby, Chen, Brian H, Huan, Tianxiao, Ying, Saixia, Munson, Peter J, Johnson, Andrew D, Levy, Daniel, O’Donnell, Christopher J
Natura: Artigo
Lingua:Inglês
Pubblicazione: 2015
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Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC8273720/
https://ncbi.nlm.nih.gov/pubmed/25685889
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/ng.3220
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