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Thanks to the safety of administration, efficiency of in vivo transduction and persistence of transgene expression, vectors based on the adeno-associated virus (AAV) are extensively utilized in both preclinical and clinical experimentation. Here we t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e1bbafe0039713655ec6a968f7df2bb3
https://hdl.handle.net/11368/2493578
https://hdl.handle.net/11368/2493578
