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A Novel Hybrid CFHR1/CFH Gene Causes Atypical Hemolytic Uremic Syndrome
BACKGROUND: Mutations in complement factor H (CFH) are associated with complement dysregulation and the development of an aggressive form of atypical hemolytic uremic syndrome (aHUS) that progresses to end-stage renal disease and in most patients has a high rate of recurrence following transplantati...
Tallennettuna:
| Julkaisussa: | Pediatr Nephrol |
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| Päätekijät: | , , , , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
2013
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4433496/ https://ncbi.nlm.nih.gov/pubmed/23880784 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00467-013-2560-2 |
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