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Rescue of the MERTK phagocytic defect in a human iPSC disease model using translational read-through inducing drugs
Inherited retinal dystrophies are an important cause of blindness, for which currently there are no effective treatments. In order to study this heterogeneous group of diseases, adequate disease models are required in order to better understand pathology and to test potential therapies. Induced plur...
| Autores principales: | , , , , , , , , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Nature Publishing Group UK
2017
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5427915/ https://www.ncbi.nlm.nih.gov/pubmed/28246391 http://dx.doi.org/10.1038/s41598-017-00142-7 |