Madelaine, R., Notwell, J. H., Skariah, G., Halluin, C., Chen, C. C., Bejerano, G., & Mourrain, P. (2018). A screen for deeply conserved non-coding GWAS SNPs uncovers a MIR-9-2 functional mutation associated to retinal vasculature defects in human. Nucleic Acids Res.
Chicago Stili AlıntıMadelaine, Romain, James H. Notwell, Gemini Skariah, Caroline Halluin, Charles C. Chen, Gill Bejerano, ve Philippe Mourrain. "A Screen for Deeply Conserved Non-coding GWAS SNPs Uncovers A MIR-9-2 functional Mutation Associated to Retinal Vasculature Defects in Human." Nucleic Acids Res 2018.
MLA AlıntıMadelaine, Romain, et al. "A Screen for Deeply Conserved Non-coding GWAS SNPs Uncovers A MIR-9-2 functional Mutation Associated to Retinal Vasculature Defects in Human." Nucleic Acids Res 2018.