AAV-mediated gene augmentation therapy of CRB1 patient-derived retinal organoids restores the histological and transcriptional retinal phenotype
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J. Wijnholds | S. Böhringer | H. Mei | Nanda Boon | C. Freund | I. Moustakas | Thilo M Buck | Xuefei Lu | C. Arendzen | Charlotte A. Andriessen | Ioannis Moustakas