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Adeno‐associated virus vectors for gene therapy—focusing on melanoma

Abstract Adeno‐Associated Virus (AAV) vectors have been found to have great potential in the field of gene therapy due to their unique properties. These nonpathogenic vectors exhibit high tissue specificity, low immunogenicity, and sustained gene expression, enhancing their efficacy for targeted del...

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Autors principals: Xingyue Wang, Miao Wei, Rui Miao, Xiujing Hao, Min Li, Wenxin Wang, Zhonglei He
Format: Artigo
Idioma:Inglês
Publicat: Wiley-VCH 2024-10-01
Col·lecció:Interdisciplinary Medicine
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Accés en línia:https://doi.org/10.1002/INMD.20240031
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