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Q41868170-E3DBF39D-C472-4D42-A7E1-75C44E504DED
Q41868170-E3DBF39D-C472-4D42-A7E1-75C44E504DED
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http://www.wikidata.org/entity/statement/Q41868170-E3DBF39D-C472-4D42-A7E1-75C44E504DED
Reducing the exome search space for mendelian diseases using genetic linkage analysis of exome genotypes.
P2860
Q41868170-E3DBF39D-C472-4D42-A7E1-75C44E504DED
BestRank
Statement
http://www.wikidata.org/entity/statement/Q41868170-E3DBF39D-C472-4D42-A7E1-75C44E504DED
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wasDerivedFrom
60b7467ec9191310994ac85576ff6cffb677bbf8
P2860
Gain-of-function mutations of ARHGAP31, a Cdc42/Rac1 GTPase regulator, cause syndromic cutis aplasia and limb anomalies