| Literature DB >> 27601107 |
Samantha Anne Nicholson1, Michael Sean Pepper.
Abstract
The ability to permanently alter or repair the human genome has been the subject of a number of science fiction films, but with the recent advent of several customisable sequence-specific endonuclease technologies, genome engineering looks set to become a clinical reality in the near future. This article discusses recent advancements in the technology called 'clustered regularly interspaced palindromic repeat (CRISPR)-associated genes' (CRISPR-Cas), the potential of CRISPR-Cas to revolutionise molecular medicine, and the ethical and regulatory hurdles facing its application.Entities:
Year: 2016 PMID: 27601107 DOI: 10.7196/SAMJ.2016.v106i9.11061
Source DB: PubMed Journal: S Afr Med J