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Article

Complement Factor H Gene Mutation Associated with Autosomal Recessive Atypical Hemolytic Uremic Syndrome

1 May 2000

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 10762557
DOI: 10.1086/302877

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Complement Factor H Gene Mutation Associated with Autosomal Recessive Atypical Hemolytic Uremic SyndromePMID 10762557Read ↗

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Comprehensive Analysis of Complement Genes in Patients with Atypical Hemolytic Uremic SyndromeSemantic proximity Read ↗

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Mutations in proteins of the alternative pathway of complement and the pathogenesis of atypical hemolytic uremic syndrome.Semantic proximity Read ↗

Clustering of Missense Mutations in the C-Terminal Region of Factor H in Atypical Hemolytic Uremic SyndromeSemantic proximity Read ↗

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