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Q33404847-4B7F1F9B-71CA-484B-98DD-D667389DFACB
Q33404847-4B7F1F9B-71CA-484B-98DD-D667389DFACB
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Statement
http://www.wikidata.org/entity/statement/Q33404847-4B7F1F9B-71CA-484B-98DD-D667389DFACB
Complement factor H-related protein 1 deficiency and factor H antibodies in pediatric patients with atypical hemolytic uremic syndrome.
P2860
Q33404847-4B7F1F9B-71CA-484B-98DD-D667389DFACB
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33404847-4B7F1F9B-71CA-484B-98DD-D667389DFACB
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wasDerivedFrom
fa57375d0cd911c2cf641d977855ea9e1c0ee762
P2860
The high frequency of complement factor H related CFHR1 gene deletion is restricted to specific subgroups of patients with atypical haemolytic uraemic syndrome.