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Identification of a mutation in complement factor H-related protein 5 in patients of Cypriot origin with glomerulonephritis
BACKGROUND: Complement is a key component of the innate immune system, and variation in genes that regulate its activation is associated with renal and other disease. We aimed to establish the genetic basis for a familial disorder of complement regulation associated with persistent microscopic haema...
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| Autors principals: | , , , , , , , , , , , , , , , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Lancet Publishing Group
2010
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2935536/ https://ncbi.nlm.nih.gov/pubmed/20800271 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/S0140-6736(10)60670-8 |
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