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Q33393852-2876A714-8AE5-4B43-A3FC-25562D914104
Q33393852-2876A714-8AE5-4B43-A3FC-25562D914104
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33393852-2876A714-8AE5-4B43-A3FC-25562D914104
Disease-associated N-terminal complement factor H mutations perturb cofactor and decay-accelerating activities.
P2860
Q33393852-2876A714-8AE5-4B43-A3FC-25562D914104
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33393852-2876A714-8AE5-4B43-A3FC-25562D914104
rank
NormalRank
type
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Statement
wasDerivedFrom
40ae0eaeda572b083cc74b966e662cbc0b796ad2
P2860
Mutations in factor H reduce binding affinity to C3b and heparin and surface attachment to endothelial cells in hemolytic uremic syndrome.