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Q33402007-35ED4C72-1B1C-4A2F-99CC-53329C7B626C
Q33402007-35ED4C72-1B1C-4A2F-99CC-53329C7B626C
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http://www.wikidata.org/entity/statement/Q33402007-35ED4C72-1B1C-4A2F-99CC-53329C7B626C
Increasing evidence that genetic variation in complement factor H related 5 (CFHR5) causes disease: a commentary on 'Atypical haemolytic uremic syndrome and genetic aberrations in the complement factor-H-related 5 gene'.
P2860
Q33402007-35ED4C72-1B1C-4A2F-99CC-53329C7B626C
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33402007-35ED4C72-1B1C-4A2F-99CC-53329C7B626C
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wasDerivedFrom
8b98d61fb2c251263c5e0c19e657cfcb38fe73ad
P2860
Variations in the complement regulatory genes factor H (CFH) and factor H related 5 (CFHR5) are associated with membranoproliferative glomerulonephritis type II (dense deposit disease)