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HARVARD Citation
Esposito, F. et al. (2022). Liver gene therapy with intein‐mediated F8 trans‐splicing corrects mouse haemophilia A. EMBO molecular medicine. 14 (6), p. n/a. [Online].
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Esposito, F. et al. (2022). Liver gene therapy with intein‐mediated F8 trans‐splicing corrects mouse haemophilia A. EMBO molecular medicine. 14 (6), p. n/a. [Online].