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Q33592763-26C07746-42F5-434E-B915-6C9833FA5B1B
Q33592763-26C07746-42F5-434E-B915-6C9833FA5B1B
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Statement
http://www.wikidata.org/entity/statement/Q33592763-26C07746-42F5-434E-B915-6C9833FA5B1B
The expanding spectrum of rare monogenic autoinflammatory diseases.
P2860
Q33592763-26C07746-42F5-434E-B915-6C9833FA5B1B
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33592763-26C07746-42F5-434E-B915-6C9833FA5B1B
rank
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Statement
wasDerivedFrom
4cb710a67e991ed9dd844aa104f261829dfcf5c6
P2860
A hypermorphic missense mutation in PLCG2, encoding phospholipase Cγ2, causes a dominantly inherited autoinflammatory disease with immunodeficiency.