Mol Ther. 2011 Dec;19(12):2111-3. doi: 10.1038/mt.2011.254.

Gene transfer using HACs: a key step closer to ex vivo gene therapy using autologous gene-corrected cells to treat muscular dystrophy.

Unité de Recherche en Génétique Humaine, Centre de Recherche du CHUQ and Université Laval, Quebec, Canada. jacques-p.tremblay@crchul.ulaval.ca

Supplemental Content

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Gene transfer using HACs: a key step closer to ex vivo gene therapy using autolo...
Gene transfer using HACs: a key step closer to ex vivo gene therapy using autologous gene-corrected cells to treat muscular dystrophy.
Mol Ther. 2011 Dec ;19(12):2111-3. doi: 10.1038/mt.2011.254.

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