AAV-mediated gene augmentation therapy of CRB1 patient-derived retinal organoids restores the histological and transcriptional retinal phenotype

AAV-mediated gene augmentation therapy of CRB1 patient-derived retinal organoids restores the histological and transcriptional retinal phenotype

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Bibliographic Details
Published in:Stem cell reports Vol. 18; no. 6; p. 1388
Main Authors: Boon, Nanda, Lu, Xuefei, Andriessen, Charlotte A., Moustakas, Ioannis, Buck, Thilo M., Freund, Christian, Arendzen, Christiaan H., Böhringer, Stefan, Boon, Camiel J.F., Mei, Hailiang, Wijnholds, Jan
Format: Journal Article
Language:English
Published: United States Elsevier Inc 13-06-2023
Elsevier
Online Access:Get full text
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Description
Bibliography:erratum
SourceType-Other Sources-1
content type line 63
ObjectType-Correction/Retraction-1
ISSN:2213-6711
2213-6711
DOI:10.1016/j.stemcr.2023.05.008