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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

ImmunohematologyAllelic VariantAutoimmune DiseaseGeneticsIga GlomerulonephritisHematologyImmunologyPathologyGenetic EpidemiologyHuman PolymorphismAutoimmunityHla TypingFunctional SignificanceMedicineVariant InterpretationHealth Sciences