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Q36495141-1512EE86-9947-40EF-ACCD-0FDC0840030D
Q36495141-1512EE86-9947-40EF-ACCD-0FDC0840030D
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http://www.wikidata.org/entity/statement/Q36495141-1512EE86-9947-40EF-ACCD-0FDC0840030D
Annexin A2 Enhances Complement Activation by Inhibiting Factor H
P2860
Q36495141-1512EE86-9947-40EF-ACCD-0FDC0840030D
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36495141-1512EE86-9947-40EF-ACCD-0FDC0840030D
rank
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Statement
wasDerivedFrom
387ea6d4902a4b967109b1189b17e394c16bc8a4
P2860
Hypocomplementemia discloses genetic predisposition to hemolytic uremic syndrome and thrombotic thrombocytopenic purpura: role of factor H abnormalities. Italian Registry of Familial and Recurrent Hemolytic Uremic Syndrome/Thrombotic Thrombocytopeni