TY  - GEN
AU  - Lumbreras, Javier
AU  - Subias, Marta
AU  - Espinosa, Natalia
AU  - Ferrer, Juana Maria
AU  - Arjona, Emilia
AU  - Rodriguez de Cordoba, Santiago
PY  - 2020
DO  - 10.3389/fimmu.2020.01348
SN  - 1664-3224
UR  - https://hdl.handle.net/20.500.12105/22920
AB  - 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...
LA  - eng
PB  - Frontiers Media
KW  - C3
KW  - MCP risk polymorphism
KW  - Atypical hemolytic uremic syndrome
KW  - De novomutation
KW  - Case report
KW  - Child
KW  - Male
KW  - Membrane Cofactor Protein
KW  - Mutation
KW  - Humans
KW  - Complement C3
KW  - Atypical Hemolytic Uremic Syndrome
KW  - Polymorphism, Single Nucleotide
KW  - Pedigree
TI  - The Relevance of the MCP Risk Polymorphism to the Outcome of aHUS Associated With C3 Mutations. A Case Report
TY  - research article
ER  -