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Hemophilia gene therapy comes of age

Concurrent with the development of recombinant factor replacement products, the characterization of the F9 and F8 genes over 3 decades ago allowed for the development of recombinant factor products and made the hemophilias a target disease for gene transfer. The progress of hemophilia gene therapy h...

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Shranjeno v:
Bibliografske podrobnosti
izdano v:Blood Adv
Glavni avtor: George, Lindsey A.
Format: Artigo
Jezik:Inglês
Izdano: American Society of Hematology 2017
Teme:
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC5728634/
https://ncbi.nlm.nih.gov/pubmed/29296912
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1182/bloodadvances.2017009878
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