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Highly efficient retinal gene delivery with helper-dependent adenoviral vectors

There have been significant advancements in the field of retinal gene therapy in the past several years. In particular, therapeutic efficacy has been achieved in three separate human clinical trials conducted to assess the ability of adeno-associated viruses (AAV) to treat of a type of Leber's...

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Podrobná bibliografie
Vydáno v:Genes Dis
Hlavní autoři: Lam, Simon, Cao, Huibi, Wu, Jing, Duan, Rongqi, Hu, Jim
Médium: Artigo
Jazyk:Inglês
Vydáno: Chongqing Medical University 2014
Témata:
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC4494825/
https://ncbi.nlm.nih.gov/pubmed/26161435
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.gendis.2014.09.002
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