Loss of DJ-1 elicits retinal abnormalities, visual dysfunction, and increased oxidative stress in mice

DJ-1/PARK7 mutations or deletions cause autosomal recessive early onset Parkinson’s disease (PD). Thus, DJ-1 protein has been extensively studied in brain and neurons. PD patients display visual symptoms; however, the visual symptoms specifically attributed to PD patients carrying DJ-1/PARK7 mutatio...

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Publicado no:Exp Eye Res
Main Authors: Bonilha, Vera L., Bell, Brent A., Rayborn, Mary E., Yang, Xiaoping, Kaul, Charlie, Grossman, Gregory H., Samuels, Ivy S., Hollyfield, Joe G., Xie, Chengsong, Cai, Huaibin, Shadrach, Karen G.
Formato: Artigo
Idioma:Inglês
Publicado em: 2015
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4573318/
https://ncbi.nlm.nih.gov/pubmed/26215528
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.exer.2015.07.014
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