
pmid: 25745178
In this issue of Blood, Crudele et al describe a novel study of adeno-associated virus (AAV) vector-mediated gene therapy that induced immune tolerance to factor IX (FIX) in a hemophilia B (HB) dog with previously formed anti-FIX inhibitor antibodies (IAs).
Factor IX, Male, Animals, Humans, Genetic Therapy, Hemophilia B
Factor IX, Male, Animals, Humans, Genetic Therapy, Hemophilia B
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