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Q38783519-F22FBAD0-7B17-40E8-8D1A-4FCE918F1221
Q38783519-F22FBAD0-7B17-40E8-8D1A-4FCE918F1221
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http://www.wikidata.org/entity/statement/Q38783519-F22FBAD0-7B17-40E8-8D1A-4FCE918F1221
A rare case: childhood-onset C3 glomerulonephritis due to homozygous factor H deficiency.
P2860
Q38783519-F22FBAD0-7B17-40E8-8D1A-4FCE918F1221
BestRank
Statement
http://www.wikidata.org/entity/statement/Q38783519-F22FBAD0-7B17-40E8-8D1A-4FCE918F1221
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wasDerivedFrom
0507bc51336c7744ba8b3db7d48515434f393ce4
P2860
The high frequency of complement factor H related CFHR1 gene deletion is restricted to specific subgroups of patients with atypical haemolytic uraemic syndrome.