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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Detalles Bibliográficos
Autores principales: Lumbreras, Javier, Subias, Marta, Espinosa, Natalia, Ferrer, Juana María, Arjona, Emilia, Rodríguez de Córdoba, Santiago
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Immunology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7381106/
https://www.ncbi.nlm.nih.gov/pubmed/32765494
http://dx.doi.org/10.3389/fimmu.2020.01348

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7381106/
https://www.ncbi.nlm.nih.gov/pubmed/32765494
http://dx.doi.org/10.3389/fimmu.2020.01348

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