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2005 | 1 |
2011 | 1 |
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Muscle-directed gene therapy for hemophilia B with more efficient and less immunogenic AAV vectors.
J Thromb Haemost. 2011 Oct;9(10):2009-19. doi: 10.1111/j.1538-7836.2011.04491.x.
J Thromb Haemost. 2011.
PMID: 21883883
Free PMC article.
Sustained correction of disease in naive and AAV2-pretreated hemophilia B dogs: AAV2/8-mediated, liver-directed gene therapy.
Wang L, Calcedo R, Nichols TC, Bellinger DA, Dillow A, Verma IM, Wilson JM.
Wang L, et al.
Blood. 2005 Apr 15;105(8):3079-86. doi: 10.1182/blood-2004-10-3867. Epub 2005 Jan 6.
Blood. 2005.
PMID: 15637142
Free article.
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