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Crystal structure of the globular domain of C1QTNF5: Implications for late-onset retinal macular degeneration
Autosomal dominant late-onset retinal macular degeneration (L-ORMD) is caused by a single S163R mutation in the C1q and tumor necrosis factor-related protein 5 (C1QTNF5) gene. The C1QTNF5 gene encodes a secreted and membrane-associated protein involved in adhesion of retinal pigmented epithelial cel...
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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/PMC3496058/ https://ncbi.nlm.nih.gov/pubmed/22892318 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.jsb.2012.07.011 |
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