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17.09.2019
21:09 ScienceDaily.comGene editing enables researchers to correct mutation in muscle stem cells in DMD model (1)

Duchenne muscular dystrophy (DMD) is a rare but devastating genetic disorder that causes muscle loss and physical impairments. Researchers have shown in a mouse study that the powerful gene editing technique known as CRISPR may provide the means for lifelong correction of the genetic mutation responsible for the disorder.