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Paul-Smith, M., Gelinas, J., Pytel, K., Chan, M., Meng, C., Cammack, L., Cameron, L., Moran, C., Pringle, I., Davies, L., Inoue, M., Hasegawa, M., Hyde, S., Gill, D., Alton, E., & Griesenbach, U. (n.d.). s127 Gene therapy for alpha-1-antitrypsin deficiency using a pseudotyped lentivirus vector. Thorax, 70, A72–A73. http://access.bl.uk/ark:/81055/vdc_100135559476.0x00002e