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Q46022690-1CBEAAA9-B63F-4B5F-B546-F45B51800114
Q46022690-1CBEAAA9-B63F-4B5F-B546-F45B51800114
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http://www.wikidata.org/entity/statement/Q46022690-1CBEAAA9-B63F-4B5F-B546-F45B51800114
Complement factor H in AMD: Bridging genetic associations and pathobiology.
P2860
Q46022690-1CBEAAA9-B63F-4B5F-B546-F45B51800114
BestRank
Statement
http://www.wikidata.org/entity/statement/Q46022690-1CBEAAA9-B63F-4B5F-B546-F45B51800114
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7f6e4d9b68e7d0100a636422c994448ada08bff1
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.