Hu, C., Cela, R. G., Suzuki, M., Lee, B., & Lipshutz, G. S. (2011). Neonatal helper-dependent adenoviral vector gene therapy mediates correction of hemophilia A and tolerance to human factor VIII. National Academy of Sciences.
Trích dẫn kiểu ChicagoHu, Chuhong, Racel G. Cela, Masataka Suzuki, Brendan Lee, và Gerald S. Lipshutz. Neonatal Helper-dependent Adenoviral Vector Gene Therapy Mediates Correction of Hemophilia A and Tolerance to Human Factor VIII. National Academy of Sciences, 2011.
Trích dẫn MLAHu, Chuhong, et al. Neonatal Helper-dependent Adenoviral Vector Gene Therapy Mediates Correction of Hemophilia A and Tolerance to Human Factor VIII. National Academy of Sciences, 2011.
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