A nonhuman primate model of inherited retinal disease
Inherited retinal degenerations are a common cause of untreatable blindness worldwide, with retinitis pigmentosa and cone dystrophy affecting approximately 1 in 3500 and 1 in 10,000 individuals, respectively. A major limitation to the development of effective therapies is the lack of availability of...
Tallennettuna:
| Päätekijät: | , , , , , , , , , , , , , , , , , , , , , |
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| Aineistotyyppi: | Artigo |
| Kieli: | englanti |
| Julkaistu: |
2019
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| Linkit: | https://doi.org/10.1172/jci123980 |
| Tagit: |
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