Characterizing human regulatory genetic variation using CRISPR/Cas9 genome editing
Rare gene-disrupting variants and common regulatory variants play key roles in rare and common disease, respectively. These variants are of great interest for investigation into genetic contributions to disease, but experimental methods to validate their impact on gene expression levels are lacking....
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| Language: | English |
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2020
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| Online Access: | https://doi.org/10.7916/d8-h4zz-2953 |