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The future of retinal gene therapy: evolving from subretinal to intravitreal vector delivery

Inherited retinal degenerations are a leading and untreatbale cause of blindness, and as such they are targets for gene therapy. Numerous gene therapy treatments have progressed from laboratory research to clinical trails, and a pioneering gene therapy received the first ever FDA approval for treati...

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Detalhes bibliográficos
Publicado no:Neural Regen Res
Main Authors: Ross, Maya, Ofri, Ron
Formato: Artigo
Idioma:Inglês
Publicado em: Wolters Kluwer - Medknow 2021
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC8328774/
https://ncbi.nlm.nih.gov/pubmed/33510064
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/1673-5374.306063
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