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Complement modulation in the retinal pigment epithelium rescues photoreceptor degeneration in a mouse model of Stargardt disease

Recessive Stargardt macular degeneration (STGD1) is caused by mutations in the gene for the ABCA4 transporter in photoreceptor outer segments. STGD1 patients and Abca4(−/−) (STGD1) mice exhibit buildup of bisretinoid-containing lipofuscin pigments in the retinal pigment epithelium (RPE), increased o...

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Dades bibliogràfiques
Publicat a:Proc Natl Acad Sci U S A
Autors principals: Lenis, Tamara L., Sarfare, Shanta, Jiang, Zhichun, Lloyd, Marcia B., Bok, Dean, Radu, Roxana A.
Format: Artigo
Idioma:Inglês
Publicat: National Academy of Sciences 2017
Matèries:
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC5393232/
https://ncbi.nlm.nih.gov/pubmed/28348233
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.1620299114
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