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Rescue of the Stargardt phenotype in Abca4 knockout mice through inhibition of vitamin A dimerization

Stargardt disease, an ATP-binding cassette, subfamily A, member 4 (ABCA4)-related retinopathy, is a genetic condition characterized by the accelerated accumulation of lipofuscin in the retinal pigment epithelium, degeneration of the neuroretina, and loss of vision. No approved treatment exists. Here...

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Detalles Bibliográficos
Publicado en:Proc Natl Acad Sci U S A
Autores principales: Charbel Issa, Peter, Barnard, Alun R., Herrmann, Philipp, Washington, Ilyas, MacLaren, Robert E.
Formato: Artigo
Lenguaje:Inglês
Publicado: National Academy of Sciences 2015
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Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC4500285/
https://ncbi.nlm.nih.gov/pubmed/26106163
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.1506960112
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