Biotechnology A CRISPR cure for Duchenne muscular dystrophy is closer after a trial in dogs Treating a fatal muscle disease could be the next major advance for gene editing. by Antonio Regalado 2018-08-24T17:26:00-04:00
Rewriting Life Doctors Plan Bold Test of Gene Therapy on Boys with Muscular Dystrophy How an unusual medical case in the 1990s provided a clue for how to treat a fatal muscle disease. by Antonio Regalado 2017-08-17T00:00:00-04:00
Biotechnology Startup Aims to Treat Muscular Dystrophy with CRISPR Patients groups are backing gene-editing as potential “home run” against disease. by Antonio Regalado 2017-02-27T12:14:00-05:00
