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Article

A novel hybrid CFHR1/CFH gene causes atypical hemolytic uremic syndrome

24 Jul 2013

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 23880784
DOI: 10.1007/s00467-013-2560-2

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A novel hybrid CFHR1/CFH gene causes atypical hemolytic uremic syndromePMID 23880784Read ↗

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A Novel Atypical Hemolytic Uremic Syndrome–Associated Hybrid CFHR1/CFH Gene Encoding a Fusion Protein That Antagonizes Factor H–Dependent Complement RegulationSemantic proximity Read ↗

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Case report: A family of atypical hemolytic uremic syndrome involving a CFH::CFHR1 fusion gene and CFHR3-1-4-2 gene duplication.Semantic proximity Read ↗

Familial Atypical Hemolytic Uremic Syndrome with Positive pS1191L (c.3572C> T) Mutation in CFH A Single-Center ExperienceSemantic proximity Read ↗

Atypical haemolytic uraemic syndrome associated with a hybrid complement gene.Semantic proximity Read ↗

A novel CFHR1-CFHR5 hybrid leads to a familial dominant C3 glomerulopathySemantic proximity Read ↗

CFHR Gene Variations Provide Insights in the Pathogenesis of the Kidney Diseases Atypical Hemolytic Uremic Syndrome and C3 Glomerulopathy.Semantic proximity Read ↗

Deletion of complement factor H-related genes CFHR1 and CFHR3 is associated with atypical hemolytic uremic syndrome.Semantic proximity Read ↗

Atypical hemolytic uremic syndrome: Korean pediatric series.Semantic proximity Read ↗

Clinical and Genetic Characteristics of Atypical Hemolytic Uremic Syndrome in Children: A Chinese Cohort Study.Semantic proximity Read ↗

Genetic analysis and functional characterization of novel mutations in a series of patients with atypical hemolytic uremic syndrome.Semantic proximity Read ↗

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