Crispr Offers New Line Of Attack On Muscular Dystrophy
Using CRISPR gene editing techniques, scientists in Germany and the United States have worked to create a corrective technique for Duchenne muscular dystrophy (DMD) mutations. The scientists say their work with CRISPR is simpler and more efficient than methods current methods trying to correct the underlying genetic basis of the disease.DMD is one of the nine types of muscular dystrophy. It generally effects boys and starts weakening muscles as early as age 3....