Abnormalities of immune complex processing in systemic lupus erythematosus
Heterozygous deficiency of C4A is a common inherited abnormality in patients with SLE who also acquire a reduction of erythrocyte (E) complement receptor type 1 (CR1) numbers. These factors could contribute to disease expression by reducing the efficiency of complement and ECR1 mediated mechanisms f...
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University of Edinburgh
1992
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| Online Access: | http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.652014 |