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AAV-mediated gene augmentation therapy restores critical ... | ResearchHub
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AAV-mediated gene augmentation therapy restores critical functions in mutant iPSC-derived PRPF31+/- cells.
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Authors
Elizabeth Brydon
•
Revital Bronstein
3 more
•
Rosario Fernández‐Godino
Published
August 8, 2019
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Preprint Server
Topics
Neuroscience
Biochemistry
Biology
Neuroscience
Biochemistry
Genetics
Molecular Biology
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DOI
10.1101/729160
License
cc-no
