Cargando...

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...

Descripción completa

Guardado en:
Detalles Bibliográficos
Publicado en:Haemophilia
Autores principales: Cantore, Alessio, Naldini, Luigi
Formato: Artigo
Lenguaje:Inglês
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea: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
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!