Emerging Issues in AAV-Mediated In Vivo Gene Therapy

In recent years, the number of clinical trials in which adeno-associated virus (AAV) vectors have been used for in vivo gene transfer has steadily increased. The excellent safety profile, together with the high efficiency of transduction of a broad range of target tissues, has established AAV vector...

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Detalles Bibliográficos
Autores principales: Colella, Pasqualina, Ronzitti, Giuseppe, Mingozzi, Federico
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society of Gene & Cell Therapy 2017
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5758940/
https://www.ncbi.nlm.nih.gov/pubmed/29326962
http://dx.doi.org/10.1016/j.omtm.2017.11.007

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5758940/
https://www.ncbi.nlm.nih.gov/pubmed/29326962
http://dx.doi.org/10.1016/j.omtm.2017.11.007

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