Neuromuscular disease: Genome editing shows promise in an in vivo model of Duchenne muscular dystrophy
Nat Rev Neurol
.
2016 Feb;12(2):63.
doi: 10.1038/nrneurol.2016.4.
Epub 2016 Jan 18.
Author
Heather Wood
PMID:
26782331
DOI:
10.1038/nrneurol.2016.4
No abstract available
Publication types
Comment
MeSH terms
Animals
CRISPR-Cas Systems / genetics*
Dystrophin / genetics*
Genome*
Humans
Male
Muscular Dystrophy, Duchenne / genetics*
Mutation*
Substances
Dystrophin