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Q50441391-1855F977-1A2A-4A06-914E-18506F868335
Q50441391-1855F977-1A2A-4A06-914E-18506F868335
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http://www.wikidata.org/entity/statement/Q50441391-1855F977-1A2A-4A06-914E-18506F868335
Novel missense mutation in DLL4 in a Japanese sporadic case of Adams-Oliver syndrome.
P2860
Q50441391-1855F977-1A2A-4A06-914E-18506F868335
BestRank
Statement
http://www.wikidata.org/entity/statement/Q50441391-1855F977-1A2A-4A06-914E-18506F868335
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wasDerivedFrom
b4ad51e9b520c1c316a0199387e5e00c683acb78
P2860
Gain-of-function mutations of ARHGAP31, a Cdc42/Rac1 GTPase regulator, cause syndromic cutis aplasia and limb anomalies