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Retinal Phenotype in the rd9 Mutant Mouse, a Model of X-Linked RP
Retinal degeneration 9 (rd9) mice carry a mutation in the retina specific “Retinitis Pigmentosa GTPase Regulator (RPGR)” Open Reading Frame (ORF) 15 gene, located on the X chromosome and represent a rare model of X-linked Retinitis Pigmentosa (XLRP), a common and severe form of retinal degeneration...
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| Publicado en: | Front Neurosci |
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| Autores principales: | , , , , , |
| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
Frontiers Media S.A.
2019
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| Materias: | |
| Acceso en línea: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6761883/ https://ncbi.nlm.nih.gov/pubmed/31607844 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fnins.2019.00991 |
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