Recently, a form of advanced gene-editing technology known as CRISPR has opened up new avenues of genetic experimentation. Its elaborate chemical structure means producers have to rely on proteins from inside mice cells to cultivate the drug. The condition is caused by a rare genetic mutation and cannot be treated using regular gene therapy. 7 Gene therapy in one eye enhances vision in bothScientists have discovered a form of gene therapy for sight loss that, when injected into one eye, improves vision in both. As part of a recent trial, 37 patients with LHON received gene therapy injections into one of their eyes.

Source: The Nation April 29, 2021 06:56 UTC