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Chapter 61: Photoreceptor Cell Degeneration in Abcr(−/−) Mice

Mice harboring a null mutation in Abca4/Abcr serve as a model of autosomal recessive Stargardt disease. Consistent with the human retinal disorder, deficiency in Abcr is associated with substantial accumulations of lipofuscin pigments in retinal pigment epithelial (RPE) cells. To observe for photore...

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Detalhes bibliográficos
Main Authors: Wu, Li, Nagasaki, Taka, Sparrow, Janet R.
Formato: Artigo
Idioma:Inglês
Publicado em: 2010
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2914303/
https://ncbi.nlm.nih.gov/pubmed/20238056
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/978-1-4419-1399-9_61
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