Highly sensitive measurements of disease progression in rare disorders: Developing and validating a multimodal model of retinal degeneration in Stargardt disease

BACKGROUND: Each inherited retinal disorder is rare, but together, they affect millions of people worldwide. No treatment is currently available for these blinding diseases, but promising new options—including gene therapy—are emerging. Arguably, the most prevalent retinal dystrophy is Stargardt dis...

Szczegółowa specyfikacja

Opis bibliograficzny
Główni autorzy: Lambertus, Stanley, Bax, Nathalie M., Fakin, Ana, Groenewoud, Joannes M. M., Klevering, B. Jeroen, Moore, Anthony T., Michaelides, Michel, Webster, Andrew R., van der Wilt, Gert Jan, Hoyng, Carel B.
Format: Online Artykuł Texto
Język:English
Wydane: Public Library of Science 2017
Hasła przedmiotowe:
Research Article
Dostęp online:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5371327/
https://www.ncbi.nlm.nih.gov/pubmed/28355279
http://dx.doi.org/10.1371/journal.pone.0174020

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5371327/
https://www.ncbi.nlm.nih.gov/pubmed/28355279
http://dx.doi.org/10.1371/journal.pone.0174020

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