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The F220C and F45L rhodopsin mutations identified in retinitis pigmentosa patients do not cause pathology in mice
Retinitis pigmentosa is a retinal degenerative disease that leads to blindness through photoreceptor loss. Rhodopsin is the most frequently mutated protein in this disease. While many rhodopsin mutations have well-understood consequences that lead to cell death, the disease association of several rh...
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| Publicado no: | Sci Rep |
|---|---|
| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Nature Publishing Group UK
2020
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7200662/ https://ncbi.nlm.nih.gov/pubmed/32371886 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41598-020-64437-y |
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