Sustained Expression of Therapeutic Level of Factor IX in Hemophilia B Dogs by AAV-Mediated Gene Therapy in Liver
Author:
Publisher
Elsevier BV
Subject
Drug Discovery,Pharmacology,Genetics,Molecular Biology,Molecular Medicine
Reference19 articles.
1. Problems and prospects in gene therapy for hemophilia;Herzog;Curr. Opin. Hematol.,1998
2. Gene therapy for the hemophilias;Walter;Adv. Vet. Med.,1997
3. Adeno-associated virus vectors and hematology;Russell;Blood,1999
4. Gene therapy for the hemophilias;Kay;Proc. Natl. Acad. Sci. USA,1999
5. Persistent and therapeutic concentrations of human factor IX in mice after hepatic gene transfer of recombinant AAV vectors;Snyder;Nat. Genet.,1997
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