Published in
Cell Press, Molecular Therapy, 2(29), p. 822-837, 2021
DOI: 10.1016/j.ymthe.2020.09.001
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In vivo HSC gene therapy using a bi-modular HDAd5/35++ vector cures Sickle Cell Disease in a mouse model.
Journal article published in 2020 by
Chang Li,
Hongjie Wang,
Aphrodite Georgakopoulou,
Sucheol Gil,
Evangelia Yannaki,
André Lieber
This paper was not found in any repository, but could be made available legally by the author.
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