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AAV-mediated gene augmentation therapy of CRB1 patient-derived retinal organoids restores the histological and transcriptional retinal phenotype
- All authors
- Boon, N.; Lu, X.F.; Andriessen, C.A.; Moustakas, I.; Buck, T.M.; Freund, C.; Arendzen, C.H.; Böhringer, S.; Boon, C.J.F.; Mei, H.L.; Wijnholds, J.
- Date
- 2023-05-09
- Journal
- Stem Cell Reports
- Volume
- 18
- Issue
- 5
- Pages
- 1123 - 1137