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Q24296397-2D0F5204-DB3D-4253-8F19-E76F9F7D1EF8
Q24296397-2D0F5204-DB3D-4253-8F19-E76F9F7D1EF8
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http://www.wikidata.org/entity/statement/Q24296397-2D0F5204-DB3D-4253-8F19-E76F9F7D1EF8
Gain-of-function mutations in RIT1 cause Noonan syndrome, a RAS/MAPK pathway syndrome
P2860
Q24296397-2D0F5204-DB3D-4253-8F19-E76F9F7D1EF8
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24296397-2D0F5204-DB3D-4253-8F19-E76F9F7D1EF8
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wasDerivedFrom
bc0db50172d19449cdf594bc5fa8f78c02d8b01a
P2860
A restricted spectrum of NRAS mutations causes Noonan syndrome