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Q28263131-F96E4604-AFF0-4CCF-869E-321871EE1107
Q28263131-F96E4604-AFF0-4CCF-869E-321871EE1107
BestRank
Statement
http://www.wikidata.org/entity/statement/Q28263131-F96E4604-AFF0-4CCF-869E-321871EE1107
Mutations in complement factor I as found in atypical hemolytic uremic syndrome lead to either altered secretion or altered function of factor I
P2860
Q28263131-F96E4604-AFF0-4CCF-869E-321871EE1107
BestRank
Statement
http://www.wikidata.org/entity/statement/Q28263131-F96E4604-AFF0-4CCF-869E-321871EE1107
rank
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type
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Statement
wasDerivedFrom
2f346d1802a06fc6aa1cc3b6cd354de0c300f428
P2860
Mutations in factor H reduce binding affinity to C3b and heparin and surface attachment to endothelial cells in hemolytic uremic syndrome.