Abstract：
:Myriad strategies have been explored to compensate for the lack of dystrophin or to skip mutations that cause the lethal disease Duchenne muscular dystrophy (DMD). A new study shows that gene editing strategies used by bacteria can be applied in zygotes of a mouse model of DMD to correct the genetic defect that causes muscular dystrophy (Long et al., 2014).
journal_name
Cell Metabjournal_title
Cell metabolismauthors
Tidball JG,Bertoni Cdoi
10.1016/j.cmet.2014.11.011subject
Has Abstractpub_date
2014-12-02 00:00:00pages
927-9issue
6eissn
1550-4131issn
1932-7420pii
S1550-4131(14)00508-7journal_volume
20pub_type
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