Single-Base Pair Genome Editing in Human Cells by Using Site-Specific Endonucleases
Genome-wide association studies have identified numerous single-nucleotide polymorphisms (SNPs) associated with human diseases or phenotypes. However, causal relationships between most SNPs and the associated disease have not been established, owing to technical challenges such as unavailability of...
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| Format: | Online |
| Language: | English |
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MDPI
2015
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| Online Access: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4613245/ |