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Q37112471-293A5D73-CA28-47D2-BC9B-2FAC5F4F7C35
Q37112471-293A5D73-CA28-47D2-BC9B-2FAC5F4F7C35
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37112471-293A5D73-CA28-47D2-BC9B-2FAC5F4F7C35
Noonan syndrome cardiac defects are caused by PTPN11 acting in endocardium to enhance endocardial-mesenchymal transformation.
P2860
Q37112471-293A5D73-CA28-47D2-BC9B-2FAC5F4F7C35
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37112471-293A5D73-CA28-47D2-BC9B-2FAC5F4F7C35
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wasDerivedFrom
e7f0541520ba2a281cd870b7b0b881318c79b6ac
P2860
Noonan syndrome mutation Q79R in Shp2 increases proliferation of valve primordia mesenchymal cells via extracellular signal-regulated kinase 1/2 signaling.