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The Relevance of the MCP Risk Polymorphism to the Outcome of aHUS Associated With C3 Mutations. A Case Report

Thrombotic microangiopathy (TMA) has different etiological causes, and not all of them are well understood. In atypical hemolytic uremic syndrome (aHUS), the TMA is caused by the complement dysregulation associated with pathogenic mutations in complement components and its regulators. Here, we descr...

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Detalhes bibliográficos
Publicado no:Front Immunol
Main Authors: Lumbreras, Javier, Subias, Marta, Espinosa, Natalia, Ferrer, Juana María, Arjona, Emilia, Rodríguez de Córdoba, Santiago
Formato: Artigo
Idioma:Inglês
Publicado em: Frontiers Media S.A. 2020
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC7381106/
https://ncbi.nlm.nih.gov/pubmed/32765494
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fimmu.2020.01348
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