The Relevance of the MCP Risk Polymorphism to the Outcome of aHUS Associated With C3 Mutations. A Case Report
Author:
Publisher
Frontiers Media SA
Subject
Immunology,Immunology and Allergy
Reference24 articles.
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2. Complement: a key system for immune surveillance and homeostasis;Ricklin;Nat Immunol.,2010
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4. Familial haemolytic uraemic syndrome and an MCP mutation;Noris;Lancet.,2003
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1. Atypical hemolytic uremic syndrome: genetically-based insights into pathogenesis through an analysis of the complement regulator CD46;Annals of Blood;2023-09
2. The Rationale of Complement Blockade of the MCPggaac Haplotype following Atypical Hemolytic Uremic Syndrome of Three Southeastern European Countries with a Literature Review;International Journal of Molecular Sciences;2023-08-22
3. The use of the drug Elizaria – a biosimilar of the original eculizumab in atypical hemolytic-uremic syndrome due to mutation of the С3 gene in children: clinical observation and literature review;Nephrology (Saint-Petersburg);2023-03-08
4. Membrane cofactor protein (MCP; CD46): deficiency states and pathogen connections;Current Opinion in Immunology;2021-10
5. A Novel Homozygous In-Frame Deletion in Complement Factor 3 Underlies Early-Onset Autosomal Recessive Atypical Hemolytic Uremic Syndrome - Case Report;Frontiers in Immunology;2021-06-24
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