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Q33375335-4E2A4386-D7D5-4943-B4B6-F3529B20A01A
Q33375335-4E2A4386-D7D5-4943-B4B6-F3529B20A01A
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http://www.wikidata.org/entity/statement/Q33375335-4E2A4386-D7D5-4943-B4B6-F3529B20A01A
Spontaneous hemolytic uremic syndrome triggered by complement factor H lacking surface recognition domains.
P2860
Q33375335-4E2A4386-D7D5-4943-B4B6-F3529B20A01A
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33375335-4E2A4386-D7D5-4943-B4B6-F3529B20A01A
rank
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type
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wasDerivedFrom
cd818ffb43107f86c53e8c9bab79a428b2268a0a
P2860
Mutations in factor H reduce binding affinity to C3b and heparin and surface attachment to endothelial cells in hemolytic uremic syndrome.