Breakthrough offers hope to those with Duchenne muscular dystrophy
by Tim Radford and agency from on (#Z94Z)
Researchers have managed to halt the progression of DMD in mice using a recently developed gene-editing technique
Gene-editing injections could one day offer hope to those with the inherited disease Duchenne muscular dystrophy, research suggests.
Researchers were able to halt the progression of DMD in adult mice using a recently developed technique that has been hailed as the scientific breakthrough of 2015.
