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

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Detalles Bibliográficos
Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Correction
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10277829/
https://www.ncbi.nlm.nih.gov/pubmed/37315526
http://dx.doi.org/10.1016/j.stemcr.2023.05.008

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10277829/
https://www.ncbi.nlm.nih.gov/pubmed/37315526
http://dx.doi.org/10.1016/j.stemcr.2023.05.008

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