Key challenges in bringing CRISPR-mediated somatic cell therapy into the clinic
Editorial summary Genome editing using clustered regularly interspersed short palindromic repeats (CRISPR) and CRISPR-associated proteins offers the potential to facilitate safe and effective treatment of genetic diseases refractory to other types of intervention. Here, we identify some of the major...
Main Authors: | , , , , , , , , , , , , , , , , , , , , , , , , , |
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Format: | Article |
Language: | English |
Published: |
BMC
2017-09-01
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Series: | Genome Medicine |
Online Access: | http://link.springer.com/article/10.1186/s13073-017-0475-4 |