A two-step gene therapy platform combining codon-optimized hOTC mRNA delivered via lipid nanoparticles (LNPs) with CRISPR/Cas9-mediated gene targeting to permanently correct early-onset severe ornithine transcarbamylase ...
Innovative liver-directed gene therapy aims to treat early and late-onset Fabry disease by enabling hepatocytes to produce alpha-galactosidase A continuously. This approach promises to overcome limitations of current the...