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A screen for deeply conserved non-coding GWAS SNPs uncovers a MIR-9-2 functional mutation associated to retinal vasculature defects in human
Thousands of human disease-associated single nucleotide polymorphisms (SNPs) lie in the non-coding genome, but only a handful have been demonstrated to affect gene expression and human biology. We computationally identified risk-associated SNPs in deeply conserved non-exonic elements (CNEs) potentia...
Autores principales: | Madelaine, Romain, Notwell, James H, Skariah, Gemini, Halluin, Caroline, Chen, Charles C, Bejerano, Gill, Mourrain, Philippe |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5909433/ https://www.ncbi.nlm.nih.gov/pubmed/29518216 http://dx.doi.org/10.1093/nar/gky166 |
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