Genetic mutation in mice treatable with CRISPR-Gold gene-editing technology – Daily Californian
Daily Californian |
Genetic mutation in mice treatable with CRISPR-Gold gene-editing technology
Daily Californian UC Berkeley researchers published a study Monday revealing a new way to deliver CRISPR-Cas9 gene-editing technology: using it to remove a genetic mutation causing Duchenne muscular dystrophy in mice. The study, published in Nature, was led by UC … CRISPR Nanoparticles Repair Duchenne Muscular Dystrophy Gene New Gene-Editing Techniques Might Not Be As Foolproof As We Thought CRISPR Therapeutics to Present at Investor Conferences in October |
