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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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Main Authors: | , , |
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Formato: | Artigo |
Idioma: | Inglês |
Publicado em: |
2010
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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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