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American Society of Hematology, Blood, 15(125), p. 2316-2318, 2015

DOI: 10.1182/blood-2015-02-625285

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Mutations in complement C3 from aHUS patients

Journal article published in 2015 by Gregers R. Andersen ORCID
This paper is made freely available by the publisher.
This paper is made freely available by the publisher.

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Abstract

In this issue of Blood, Schramm et al demonstrate that the majority of mutations in complement C3 identified in atypical hemolytic uremic syndrome (aHUS) patients cause dysregulation in the alternative pathway of complement.