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Q36559231-B69B672A-A092-41BC-B36D-8FC487B51AA2
Q36559231-B69B672A-A092-41BC-B36D-8FC487B51AA2
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36559231-B69B672A-A092-41BC-B36D-8FC487B51AA2
De Novo Loss-of-Function Mutations in USP9X Cause a Female-Specific Recognizable Syndrome with Developmental Delay and Congenital Malformations
P2860
Q36559231-B69B672A-A092-41BC-B36D-8FC487B51AA2
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36559231-B69B672A-A092-41BC-B36D-8FC487B51AA2
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type
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wasDerivedFrom
5cad5c2eff1937e0772fa7c67abb0cd56ff51260
P2860
Variable escape from X-chromosome inactivation: identifying factors that tip the scales towards expression