A novel mutation in complement 2 accompanied by susceptibility variants in C3 glomerulonephritis: A case study
Background: C3 glomerulonephritis is a rare, chronic disease characterized by C3c-dominant staining on renal biopsy and is caused by inherited or acquired alternative complement pathway dysregulation. Case presentation: Here, we reported a 36-year-old man presenting with nephritic syndrome and norma...
Kaydedildi:
| Asıl Yazarlar: | , , , , , |
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| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
Elsevier
2019-11-01
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| Seri Bilgileri: | Nefrología (English Edition) |
| Online Erişim: | http://www.sciencedirect.com/science/article/pii/S2013251419301555 |
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