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Q33373674-5E927A1C-5FB6-4C58-9F27-CC5FBC4F5932
Q33373674-5E927A1C-5FB6-4C58-9F27-CC5FBC4F5932
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http://www.wikidata.org/entity/statement/Q33373674-5E927A1C-5FB6-4C58-9F27-CC5FBC4F5932
Gain-of-function mutations in complement factor B are associated with atypical hemolytic uremic syndrome.
P2860
Q33373674-5E927A1C-5FB6-4C58-9F27-CC5FBC4F5932
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33373674-5E927A1C-5FB6-4C58-9F27-CC5FBC4F5932
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type
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wasDerivedFrom
3831d17cafd98f0e0b4bf4494b2bc8e93e24e73c
P2860
Mutations in factor H reduce binding affinity to C3b and heparin and surface attachment to endothelial cells in hemolytic uremic syndrome.