Successful Transduction with AAV Vectors after Selective Depletion of Anti-AAV Antibodies by Immunoadsorption
Author:
Funder
NHLBI
Leducq Foundation
Publisher
Elsevier BV
Subject
Genetics,Molecular Biology,Molecular Medicine
Reference25 articles.
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3. Recombinant Adeno-Associated Virus Gene Therapy in Light of Luxturna (and Zolgensma and Glybera): Where Are We, and How Did We Get Here?;Keeler;Annu. Rev. Virol.,2019
4. Hemophilia B Gene Therapy with a High-Specific-Activity Factor IX Variant;George;N. Engl. J. Med.,2017
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