CRISPR Used to Disable Defective Gene in ALS – Rare Disease Report
Rare Disease Report |
CRISPR Used to Disable Defective Gene in ALS
Rare Disease Report In historical studies, CRISPR/Cas9 technology has exhibited the ability to decrease the functionality of the mutant Dystrophin protein which has long been believed to be the underlying cause of Duchenne muscular dystrophy (DMD). Recent data from … |
