Duchenne MD Therapy by Gene Editing of Stem Cells May Be Possible in Next Decade – Muscular Dystrophy News
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Duchenne MD Therapy by Gene Editing of Stem Cells May Be Possible in Next Decade
Muscular Dystrophy News UCLA scientists have developed a potential gene therapy approach for Duchenne muscular dystrophy (DMD) using CRISPR/Cas9 technology and stem cells. If the new treatment proves successful and reaches the clinic — possibly in the next decade — it … |
