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Q33389945-E23C14F9-B0FC-49BC-A4D7-29E7BDAC948C
Q33389945-E23C14F9-B0FC-49BC-A4D7-29E7BDAC948C
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http://www.wikidata.org/entity/statement/Q33389945-E23C14F9-B0FC-49BC-A4D7-29E7BDAC948C
Genetics and complement in atypical HUS.
P2860
Q33389945-E23C14F9-B0FC-49BC-A4D7-29E7BDAC948C
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33389945-E23C14F9-B0FC-49BC-A4D7-29E7BDAC948C
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df9d7890816062a3031af187ba2cc6467cb51f8a
P2860
Factor H dysfunction in patients with atypical hemolytic uremic syndrome contributes to complement deposition on platelets and their activation.