Genome editing of F508del mutation in cystic fibrosis
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下载链接：
https://www.ncbi.nlm.nih.gov/bioproject/PRJNA646350
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资源简介：
The aim of the study is to evaluate an efficacy of genome editing using CRISPR/Cas9 for correction of F508del mutation in CFTR gene. We use several nucleases, sgRNAs and donor molecules for DNA repair and perform experiments in several cells lines, including patient-derived iPSCs
创建时间：
2020-07-15
