about
Current animal models of hemophilia: the state of the artCRISPR/Cas9-mediated genome editing via postnatal administration of AAV vector cures haemophilia B mice.Effects of FVIII immunity on hepatocyte and hematopoietic stem cell-directed gene therapy of murine hemophilia A.Adeno-associated virus (AAV) vectors in cancer gene therapy.Measuring success in hemophilia gene therapy using a factor level & outcomes yardstick.
P2860
description
2015 nî lūn-bûn
@nan
2015年の論文
@ja
2015年論文
@yue
2015年論文
@zh-hant
2015年論文
@zh-hk
2015年論文
@zh-mo
2015年論文
@zh-tw
2015年论文
@wuu
2015年论文
@zh
2015年论文
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name
New approaches to gene and cell therapy for hemophilia.
@en
type
label
New approaches to gene and cell therapy for hemophilia.
@en
prefLabel
New approaches to gene and cell therapy for hemophilia.
@en
P2093
P2860
P356
P1476
New approaches to gene and cell therapy for hemophilia
@en
P2093
P2860
P304
P356
10.1111/JTH.12926
P478
13 Suppl 1
P577
2015-06-01T00:00:00Z