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2011•Kidney InternationalRequires access

Complement factor H variants I890 and L1007 while commonly associated with atypical hemolytic uremic syndrome are polymorphisms with no functional significance

Agustín Tortajada, Sheila Pinto, Jorge Martínez-Ara, Margarita López‐Trascasa, Pilar Sánchez‐Corral, Santiago Rodrı́guez de Córdoba

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Key concepts: Atypical hemolytic uremic syndrome, Factor H, Complement factor B, Complement factor I, Haplotype, Disease, Genetics, Biology

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Complement factor H variants I890 and L1007 while commonly associated with atypical hemolytic uremic syndrome are polymorphisms with no functional significance — Research Paper | ScholarLens