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Published in 2022 at "Frontiers in Immunology"
DOI: 10.3389/fimmu.2022.975803
Abstract: Gene transfer using adeno-associated viral (AAV) vectors has made tremendous progress in the last decade and has achieved cures of debilitating diseases such as hemophilia A and B. Nevertheless, progress is still being hampered by…
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Keywords:
toxicity aav;
aav gene;
aav vectors;
gene ... See more keywords