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Identical point mutation leading to low levels of mannose binding protein and poor C3b mediated opsonisation in Chinese and Caucasian populations

Allelic VariantGenetic DisorderNatural SciencesGeneticsHuman PolymorphismCaucasian PopulationsMolecular BiologyIdentical Point MutationProtein GeneticsMolecular GeneticsGenomicsPoor C3bGene ExpressionMedicine