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Mutations in complement C3 from aHUS patients

Blood
DOI: 10.1182/blood-2015-02-625285
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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.1

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Andersen, G. R. (2015, April 9). Mutations in complement C3 from aHUS patients. Blood. American Society of Hematology. https://doi.org/10.1182/blood-2015-02-625285

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