New CRISPR-Cas9 Technique Corrects Defects Linked to Huntington’s, UCSD Study Suggests – Huntington’s Disease News
Huntington’s Disease News |
New CRISPR-Cas9 Technique Corrects Defects Linked to Huntington's, UCSD Study Suggests
Huntington’s Disease News CRISPR-Cas9 is an innovative technique designed to edit genes. The process introduces breaks in the DNA of the gene of interest, which would disable the incorrect gene. CRISPR-Cas9 can also be used to replace an incorrect gene with the correct version. Synbio Technologies Makes Breakthrough in sgRNA Libraries |
