Additional file 9 of Clinical exome analysis and targeted gene repair of the c.1354dupT variant in iPSC lines from patients with PROM1-related retinopathies exhibiting diverse phenotypes [Dataset]
Supplementary file 9: Sequencing data from IRD2’ daughter.
| Autores: | , , , , , , , , , |
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| Tipo de recurso: | conjunto de datos |
| Estado: | Versión publicada |
| Fecha de publicación: | 2024 |
| País: | España |
| Institución: | Consejo Superior de Investigaciones Científicas (CSIC) |
| Repositorio: | DIGITAL.CSIC. Repositorio Institucional del CSIC |
| OAI Identifier: | oai:digital.csic.es:10261/380220 |
| Acceso en línea: | http://hdl.handle.net/10261/380220 |
| Access Level: | acceso abierto |
| Palabra clave: | iPSC Retinal diseases PROM1 gene CD133 Retinitis pigmentosa Cone-rod dystrophy Stargardt’s type 4 disease |
| Sumario: | Supplementary file 9: Sequencing data from IRD2’ daughter. |
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