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Q36559231-E01566C5-244D-4220-B7CC-1EF526BA9FA5
Q36559231-E01566C5-244D-4220-B7CC-1EF526BA9FA5
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36559231-E01566C5-244D-4220-B7CC-1EF526BA9FA5
De Novo Loss-of-Function Mutations in USP9X Cause a Female-Specific Recognizable Syndrome with Developmental Delay and Congenital Malformations
P2860
Q36559231-E01566C5-244D-4220-B7CC-1EF526BA9FA5
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36559231-E01566C5-244D-4220-B7CC-1EF526BA9FA5
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wasDerivedFrom
5cad5c2eff1937e0772fa7c67abb0cd56ff51260
P2860
Loss of Usp9x disrupts cortical architecture, hippocampal development and TGFβ-mediated axonogenesis