New CRISPR method strategically targets gene mutations to correct DMD heart defect – New Atlas
New Atlas |
New CRISPR method strategically targets gene mutations to correct DMD heart defect
New Atlas Researchers at UT Southwestern Medical Center have developed a CRISPR technique to efficiently correct the function of heart cells in patients with Duchenne muscular dystrophy (DMD). It involves making a single cut at strategic points along patient's … |
