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WFH State‐of‐the‐art paper 2020: In vivo lentiviral vector gene therapy for haemophilia

Over the last decade, the development of new treatments for haemophilia has progressed at a very rapid pace. Despite all the promising advances in protein products, the prospect offered by gene therapy of a single potentially lifelong treatment remains attractive for people with haemophilia. Transfe...

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Dettagli Bibliografici
Pubblicato in:Haemophilia
Autori principali: Cantore, Alessio, Naldini, Luigi
Natura: Artigo
Lingua:Inglês
Pubblicazione: John Wiley and Sons Inc. 2020
Soggetti:
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC7984334/
https://ncbi.nlm.nih.gov/pubmed/32537776
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/hae.14056
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