Abstract
A FUNCTIONALLY defective molecule, immunologically similar to Factor VIII, has been found in haemophilia A patients in concentrations similar to normal, but in von Willebrand's disease the immunological concentration of Factor VIII is reduced or absent1,2. Two principal approaches have been used to detect this cross-reactive material (CRM). One method is based on the ability of plasma incubated with antibody to neutralize the anticoagulant effect of the antibody (antibody neutralization). The second group of methods involves the use of immunoprecipitation techniques.
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GRALNICK, H., COLLER, B. & MARCHESI, S. Immunological Studies of Factor VIII in Haemophilia and von Willebrand's Disease. Nature New Biology 244, 281–282 (1973). https://doi.org/10.1038/newbio244281a0
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DOI: https://doi.org/10.1038/newbio244281a0