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Q28300378-6B2D8E33-12E7-4307-A014-01328422889D
Q28300378-6B2D8E33-12E7-4307-A014-01328422889D
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Statement
http://www.wikidata.org/entity/statement/Q28300378-6B2D8E33-12E7-4307-A014-01328422889D
The development of atypical hemolytic uremic syndrome depends on complement C5
P2860
Q28300378-6B2D8E33-12E7-4307-A014-01328422889D
BestRank
Statement
http://www.wikidata.org/entity/statement/Q28300378-6B2D8E33-12E7-4307-A014-01328422889D
rank
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type
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Statement
wasDerivedFrom
4473476484fdaee70a3d7d88cae85016a2cf3f51
P2860
Mutations in factor H reduce binding affinity to C3b and heparin and surface attachment to endothelial cells in hemolytic uremic syndrome.