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Establishment of the iPSC line CUIMCi005-A from a patient with Stargardt disease for retinal organoid culture
Pathogenic variation in the ABCA4 gene is the underlying cause of Stargardt disease, the most common inherited retinal degeneration. We established an induced pluripotent stem cell line for retinal organoid research from a patient with mild disease features who is compound heterozygous for the frequ...
| Autores principales: | , , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
2022
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9801682/ https://www.ncbi.nlm.nih.gov/pubmed/36455383 http://dx.doi.org/10.1016/j.scr.2022.102973 |