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Q24613907-65292DCA-DFBD-491C-BE78-FD14A3F4A7E0
Q24613907-65292DCA-DFBD-491C-BE78-FD14A3F4A7E0
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24613907-65292DCA-DFBD-491C-BE78-FD14A3F4A7E0
Relative role of genetic complement abnormalities in sporadic and familial aHUS and their impact on clinical phenotype
P2860
Q24613907-65292DCA-DFBD-491C-BE78-FD14A3F4A7E0
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24613907-65292DCA-DFBD-491C-BE78-FD14A3F4A7E0
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wasDerivedFrom
31ad7e94e4e890bdf991690d6211675d96eed7bd
P2860
The high frequency of complement factor H related CFHR1 gene deletion is restricted to specific subgroups of patients with atypical haemolytic uraemic syndrome.