mRNA Gene Therapy Research Targeting Alpha-Galactosidase A Deficiency 2027
The Promise of a Curative Single Dose Gene Therapy Research represents the most profound potential shift in the management of this inherited condition, offering the possibility of a one-time, potentially curative treatment. Current investigations primarily utilize Adeno-Associated Virus (AAV) vectors to deliver a functional copy of the deficient GLA gene to the patient’s cells, often...
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