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Genome editing with CRISPR/Cas9 has the potential to cure debilitating genetic diseases such as Duchenne muscular dystrophy

3/18/2017

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Contributed by David Ottenheimer,
PhD student at Johns Hopkins

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  • Research Database
    • Basic Research DB
    • Medical Research DB
    • Engineering DB
  • About us
    • Our Story
    • How It Works
    • Leadership
    • Q&A
    • Contact us
  • How to Participate
    • Guideline for Researchers
    • Guideline for Editors
  • Forum
  • Tech Transfer