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Iron-mediated retinal degeneration in hemojuvelin knockout mice
Hemochromatosis is a genetic disorder of iron overload resulting from loss-of-function mutations in genes coding for the iron-regulatory proteins HFE, transferrin receptor 2, ferroportin, hepcidin, and hemojuvelin (HJV). Recent studies have established the expression of all the five genes in retina,...
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| Main Authors: | , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2012
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3710445/ https://ncbi.nlm.nih.gov/pubmed/21943374 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1042/BJ20111148 |
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