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Researchers show feasibility of stem cell-derived organoids for developing gene therapy vectors

00:21 EDT 14 Jun 2018 | News-Medical.net

A new study that compared six of the most promising adeno-associated viral gene therapy vectors in human retinal organoid models showed clear distinctions in the efficiency of gene transfer to both retinal pigment epithelial and photoreceptor cells.

Original Article: Researchers show feasibility of stem cell-derived organoids for developing gene therapy vectors

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