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Q24523983-4866686F-C9E7-43F8-82AC-0D87AED92C83
Q24523983-4866686F-C9E7-43F8-82AC-0D87AED92C83
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http://www.wikidata.org/entity/statement/Q24523983-4866686F-C9E7-43F8-82AC-0D87AED92C83
A common haplotype in the complement regulatory gene factor H (HF1/CFH) predisposes individuals to age-related macular degeneration
P2860
Q24523983-4866686F-C9E7-43F8-82AC-0D87AED92C83
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24523983-4866686F-C9E7-43F8-82AC-0D87AED92C83
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wasDerivedFrom
70b8f444f6a46c3c196995114fa172231765c91e
P2860
Complement factor H mutations and gene polymorphisms in haemolytic uraemic syndrome: the C-257T, the A2089G and the G2881T polymorphisms are strongly associated with the disease.