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Q33373674-2DBFA90A-E8B3-47D0-BC68-6B5BCCE357AD
Q33373674-2DBFA90A-E8B3-47D0-BC68-6B5BCCE357AD
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Statement
http://www.wikidata.org/entity/statement/Q33373674-2DBFA90A-E8B3-47D0-BC68-6B5BCCE357AD
Gain-of-function mutations in complement factor B are associated with atypical hemolytic uremic syndrome.
P2860
Q33373674-2DBFA90A-E8B3-47D0-BC68-6B5BCCE357AD
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33373674-2DBFA90A-E8B3-47D0-BC68-6B5BCCE357AD
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wasDerivedFrom
3831d17cafd98f0e0b4bf4494b2bc8e93e24e73c
P2860
The molecular basis of familial hemolytic uremic syndrome: mutation analysis of factor H gene reveals a hot spot in short consensus repeat 20.